Canonical Allele Identifier: CA1058132890
Gene: TNK2 HGNC NCBI

Linked Data

dbSNP Id: rs1744033541

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.195870178_195870179insA , CM000665.2:g.195870178_195870179insA GRCh38
NC_000003.11:g.195597049_195597050insA , CM000665.1:g.195597049_195597050insA GRCh37
NC_000003.10:g.197081446_197081447insA NCBI36
NG_029779.1:g.43831_43832insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000672887.2:c.1478_1479insT MANE Select ENSP00000499899.1:p.Asp495ArgfsTer?
ENST00000333602.14:c.1478_1479insT ENSP00000329425.6:p.Asp495ArgfsTer25
ENST00000381916.7:c.1667_1668insT ENSP00000371341.2:p.Asp558ArgfsTer?
ENST00000428187.7:c.1574_1575insT ENSP00000392546.1:p.Asp527ArgfsTer25
ENST00000439230.6:c.*90_*91insT ENSP00000395588.1:n.*90_*91insT
ENST00000671753.1:c.1550_1551insT ENSP00000499858.1:p.Asp519ArgfsTer?
ENST00000671767.1:c.272_273insT ENSP00000499862.1:p.Asp93ArgfsTer25
ENST00000671831.1:n.731_732insT
ENST00000672024.1:c.1478_1479insT ENSP00000500486.1:p.Asp495ArgfsTer25
ENST00000672098.1:c.8_9insT ENSP00000500684.1:p.Asp5ArgfsTer25
ENST00000672320.1:n.328_329insT
ENST00000672548.1:c.8_9insT ENSP00000500238.1:p.Asp5ArgfsTer25
ENST00000672614.1:n.3986_3987insT
ENST00000672669.1:c.8_9insT ENSP00000500276.1:p.Asp5ArgfsTer25
ENST00000672886.1:c.8_9insT ENSP00000500479.1:p.Asp5ArgfsTer25
ENST00000672887.1:c.1478_1479insT ENSP00000499899.1:p.Asp495ArgfsTer?
ENST00000673038.1:c.1574_1575insT ENSP00000500452.1:p.Asp527ArgfsTer25
ENST00000673358.1:n.1075_1076insT
ENST00000673374.1:c.*453_*454insT ENSP00000500225.1:n.*453_*454insT
ENST00000673420.1:c.1478_1479insT ENSP00000500887.1:p.Asp495ArgfsTer25
ENST00000678220.1:c.1574_1575insT ENSP00000503221.1:p.Asp527ArgfsTer25
ENST00000333602.10:c.1478_1479insT ENSP00000329425.6:p.Asp495ArgfsTer25
ENST00000381916.6:c.1667_1668insT ENSP00000371341.2:p.Asp558ArgfsTer?
ENST00000411741.1:c.413_414insT ENSP00000415126.1:p.Asp140ArgfsTer25
ENST00000416152.5:c.134_135insT ENSP00000398614.1:p.Asp47ArgfsTer?
ENST00000424563.5:c.307_308insT
ENST00000428187.5:c.1574_1575insT ENSP00000392546.1:p.Asp527ArgfsTer25
ENST00000439230.5:c.*90_*91insT ENSP00000395588.1:n.*90_*91insT
ENST00000464041.5:n.1583_1584insT
ENST00000468680.1:n.731_732insT
ENST00000478623.5:n.296_297insT
ENST00000478715.1:n.328_329insT
ENST00000481865.5:n.3986_3987insT
ENST00000489628.1:n.1075_1076insT
NM_001010938.1:c.1667_1668insT NP_001010938.1:p.Asp558ArgfsTer?
NM_001308046.1:c.1574_1575insT NP_001294975.1:p.Asp527ArgfsTer25
NM_005781.4:c.1478_1479insT NP_005772.3:p.Asp495ArgfsTer25
XM_005269268.3:c.1667_1668insT XP_005269325.1:p.Asp558ArgfsTer?
XM_005269270.3:c.1478_1479insT XP_005269327.1:p.Asp495ArgfsTer?
XM_005269274.3:c.761_762insT XP_005269331.1:p.Asp256ArgfsTer?
XM_005269275.3:c.536_537insT XP_005269332.1:p.Asp181ArgfsTer?
XM_011512317.1:c.1970_1971insT XP_011510619.1:p.Asp659ArgfsTer?
XM_011512318.1:c.1478_1479insT XP_011510620.1:p.Asp495ArgfsTer?
XM_011512319.1:c.1478_1479insT XP_011510621.1:p.Asp495ArgfsTer25
XM_011512320.1:c.1478_1479insT XP_011510622.1:p.Asp495ArgfsTer?
XM_011512321.1:c.1250_1251insT XP_011510623.1:p.Asp419ArgfsTer?
XM_011512317.3:c.1970_1971insT XP_011510619.1:p.Asp659ArgfsTer?
XM_011512318.2:c.1574_1575insT XP_011510620.2:p.Asp527ArgfsTer?
XM_011512321.2:c.1250_1251insT XP_011510623.1:p.Asp419ArgfsTer?
XM_017005508.1:c.1574_1575insT XP_016860997.1:p.Asp527ArgfsTer25
XM_017005509.1:c.1574_1575insT XP_016860998.1:p.Asp527ArgfsTer25
XM_017005510.1:c.1574_1575insT XP_016860999.1:p.Asp527ArgfsTer?
XM_024453291.1:c.1670_1671insT XP_024309059.1:p.Asp559ArgfsTer?
XM_024453292.1:c.1529_1530insT XP_024309060.1:p.Asp512ArgfsTer?
XM_024453293.1:c.1478_1479insT XP_024309061.1:p.Asp495ArgfsTer?
XM_024453294.1:c.1478_1479insT XP_024309062.1:p.Asp495ArgfsTer?
XM_024453295.1:c.1478_1479insT XP_024309063.1:p.Asp495ArgfsTer?
NM_001010938.2:c.1550_1551insT NP_001010938.2:p.Asp519ArgfsTer?
NM_001308046.2:c.1574_1575insT NP_001294975.1:p.Asp527ArgfsTer25
NM_001382271.1:c.1574_1575insT NP_001369200.1:p.Asp527ArgfsTer25
NM_001382272.1:c.1550_1551insT NP_001369201.1:p.Asp519ArgfsTer?
NM_001382273.1:c.1478_1479insT MANE Select NP_001369202.1:p.Asp495ArgfsTer?
NM_001382274.1:c.1478_1479insT NP_001369203.1:p.Asp495ArgfsTer?
NM_001382275.1:c.1574_1575insT NP_001369204.1:p.Asp527ArgfsTer?
NM_001386164.1:c.1478_1479insT NP_001373093.1:p.Asp495ArgfsTer25
NM_001387707.1:c.1574_1575insT NP_001374636.1:p.Asp527ArgfsTer?
NM_001387708.1:c.1550_1551insT NP_001374637.1:p.Asp519ArgfsTer25
NM_001387709.1:c.1478_1479insT NP_001374638.1:p.Asp495ArgfsTer25
NM_001387710.1:c.1478_1479insT NP_001374639.1:p.Asp495ArgfsTer25
NM_001387711.1:c.1478_1479insT NP_001374640.1:p.Asp495ArgfsTer25
NM_001387712.1:c.1478_1479insT NP_001374641.1:p.Asp495ArgfsTer25
NM_001387713.1:c.1478_1479insT NP_001374642.1:p.Asp495ArgfsTer25
NM_001387714.1:c.1478_1479insT NP_001374643.1:p.Asp495ArgfsTer25
NM_001387715.1:c.1550_1551insT NP_001374644.1:p.Asp519ArgfsTer25
NM_001387716.1:c.1478_1479insT NP_001374645.1:p.Asp495ArgfsTer?
NM_001387717.1:c.1478_1479insT NP_001374646.1:p.Asp495ArgfsTer?
NM_001387718.1:c.1478_1479insT NP_001374647.1:p.Asp495ArgfsTer?
NM_001387719.1:c.1478_1479insT NP_001374648.1:p.Asp495ArgfsTer25
NM_001387720.1:c.1478_1479insT NP_001374649.1:p.Asp495ArgfsTer25
NM_001387721.1:c.1478_1479insT NP_001374650.1:p.Asp495ArgfsTer25
NM_005781.5:c.1478_1479insT NP_005772.3:p.Asp495ArgfsTer25
NR_170678.1:n.1725_1726insT
NR_170679.1:n.2029_2030insT
NR_170680.1:n.1736_1737insT
NR_170681.1:n.1736_1737insT
NR_170682.1:n.2003_2004insT
NR_170683.1:n.2003_2004insT
NR_170684.1:n.1416_1417insT
NR_170685.1:n.1874_1875insT
NR_170686.1:n.1787_1788insT
NR_170687.1:n.1717_1718insT
NR_170688.1:n.2003_2004insT
NR_170689.1:n.1517_1518insT
NR_170690.1:n.1328_1329insT
NR_170691.1:n.1675_1676insT
NR_170692.1:n.1285_1286insT