Canonical Allele Identifier: CA355572791

Gene: TNK2

Linked Data

• gnomAD v4: 3-195870174-C-A
• MyVariant Identifiers: chr3:g.195597045C>A (hg19) ; chr3:g.195870174C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.195870174C>A , CM000665.2:g.195870174C>A	GRCh38
NC_000003.11:g.195597045C>A , CM000665.1:g.195597045C>A	GRCh37
NC_000003.10:g.197081442C>A	NCBI36
NG_029779.1:g.43836G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000672887.2:c.1483G>T MANE Select	ENSP00000499899.1:p.Asp495Tyr
ENST00000333602.14:c.1483G>T	ENSP00000329425.6:p.Asp495Tyr
ENST00000381916.7:c.1672G>T	ENSP00000371341.2:p.Asp558Tyr
ENST00000428187.7:c.1579G>T	ENSP00000392546.1:p.Asp527Tyr
ENST00000439230.6:c.*95G>T	ENSP00000395588.1:n.*95G>T
ENST00000671753.1:c.1555G>T	ENSP00000499858.1:p.Asp519Tyr
ENST00000671767.1:c.277G>T	ENSP00000499862.1:p.Asp93Tyr
ENST00000671831.1:n.736G>T
ENST00000672024.1:c.1483G>T	ENSP00000500486.1:p.Asp495Tyr
ENST00000672098.1:c.13G>T	ENSP00000500684.1:p.Asp5Tyr
ENST00000672320.1:n.333G>T
ENST00000672548.1:c.13G>T	ENSP00000500238.1:p.Asp5Tyr
ENST00000672614.1:n.3991G>T
ENST00000672669.1:c.13G>T	ENSP00000500276.1:p.Asp5Tyr
ENST00000672886.1:c.13G>T	ENSP00000500479.1:p.Asp5Tyr
ENST00000672887.1:c.1483G>T	ENSP00000499899.1:p.Asp495Tyr
ENST00000673038.1:c.1579G>T	ENSP00000500452.1:p.Asp527Tyr
ENST00000673358.1:n.1080G>T
ENST00000673374.1:c.*458G>T	ENSP00000500225.1:n.*458G>T
ENST00000673420.1:c.1483G>T	ENSP00000500887.1:p.Asp495Tyr
ENST00000678220.1:c.1579G>T	ENSP00000503221.1:p.Asp527Tyr
ENST00000333602.10:c.1483G>T	ENSP00000329425.6:p.Asp495Tyr
ENST00000381916.6:c.1672G>T	ENSP00000371341.2:p.Asp558Tyr
ENST00000411741.1:c.418G>T	ENSP00000415126.1:p.Asp140Tyr
ENST00000416152.5:c.139G>T	ENSP00000398614.1:p.Asp47Tyr
ENST00000424563.5:c.312G>T
ENST00000428187.5:c.1579G>T	ENSP00000392546.1:p.Asp527Tyr
ENST00000439230.5:c.*95G>T	ENSP00000395588.1:n.*95G>T
ENST00000464041.5:n.1588G>T
ENST00000468680.1:n.736G>T
ENST00000478623.5:n.301G>T
ENST00000478715.1:n.333G>T
ENST00000481865.5:n.3991G>T
ENST00000489628.1:n.1080G>T
NM_001010938.1:c.1672G>T	NP_001010938.1:p.Asp558Tyr
NM_001308046.1:c.1579G>T	NP_001294975.1:p.Asp527Tyr
NM_005781.4:c.1483G>T	NP_005772.3:p.Asp495Tyr
XM_005269268.3:c.1672G>T	XP_005269325.1:p.Asp558Tyr
XM_005269270.3:c.1483G>T	XP_005269327.1:p.Asp495Tyr
XM_005269274.3:c.766G>T	XP_005269331.1:p.Asp256Tyr
XM_005269275.3:c.541G>T	XP_005269332.1:p.Asp181Tyr
XM_011512317.1:c.1975G>T	XP_011510619.1:p.Asp659Tyr
XM_011512318.1:c.1483G>T	XP_011510620.1:p.Asp495Tyr
XM_011512319.1:c.1483G>T	XP_011510621.1:p.Asp495Tyr
XM_011512320.1:c.1483G>T	XP_011510622.1:p.Asp495Tyr
XM_011512321.1:c.1255G>T	XP_011510623.1:p.Asp419Tyr
XM_011512317.3:c.1975G>T	XP_011510619.1:p.Asp659Tyr
XM_011512318.2:c.1579G>T	XP_011510620.2:p.Asp527Tyr
XM_011512321.2:c.1255G>T	XP_011510623.1:p.Asp419Tyr
XM_017005508.1:c.1579G>T	XP_016860997.1:p.Asp527Tyr
XM_017005509.1:c.1579G>T	XP_016860998.1:p.Asp527Tyr
XM_017005510.1:c.1579G>T	XP_016860999.1:p.Asp527Tyr
XM_024453291.1:c.1675G>T	XP_024309059.1:p.Asp559Tyr
XM_024453292.1:c.1534G>T	XP_024309060.1:p.Asp512Tyr
XM_024453293.1:c.1483G>T	XP_024309061.1:p.Asp495Tyr
XM_024453294.1:c.1483G>T	XP_024309062.1:p.Asp495Tyr
XM_024453295.1:c.1483G>T	XP_024309063.1:p.Asp495Tyr
NM_001010938.2:c.1555G>T	NP_001010938.2:p.Asp519Tyr
NM_001308046.2:c.1579G>T	NP_001294975.1:p.Asp527Tyr
NM_001382271.1:c.1579G>T	NP_001369200.1:p.Asp527Tyr
NM_001382272.1:c.1555G>T	NP_001369201.1:p.Asp519Tyr
NM_001382273.1:c.1483G>T MANE Select	NP_001369202.1:p.Asp495Tyr
NM_001382274.1:c.1483G>T	NP_001369203.1:p.Asp495Tyr
NM_001382275.1:c.1579G>T	NP_001369204.1:p.Asp527Tyr
NM_001386164.1:c.1483G>T	NP_001373093.1:p.Asp495Tyr
NM_001387707.1:c.1579G>T	NP_001374636.1:p.Asp527Tyr
NM_001387708.1:c.1555G>T	NP_001374637.1:p.Asp519Tyr
NM_001387709.1:c.1483G>T	NP_001374638.1:p.Asp495Tyr
NM_001387710.1:c.1483G>T	NP_001374639.1:p.Asp495Tyr
NM_001387711.1:c.1483G>T	NP_001374640.1:p.Asp495Tyr
NM_001387712.1:c.1483G>T	NP_001374641.1:p.Asp495Tyr
NM_001387713.1:c.1483G>T	NP_001374642.1:p.Asp495Tyr
NM_001387714.1:c.1483G>T	NP_001374643.1:p.Asp495Tyr
NM_001387715.1:c.1555G>T	NP_001374644.1:p.Asp519Tyr
NM_001387716.1:c.1483G>T	NP_001374645.1:p.Asp495Tyr
NM_001387717.1:c.1483G>T	NP_001374646.1:p.Asp495Tyr
NM_001387718.1:c.1483G>T	NP_001374647.1:p.Asp495Tyr
NM_001387719.1:c.1483G>T	NP_001374648.1:p.Asp495Tyr
NM_001387720.1:c.1483G>T	NP_001374649.1:p.Asp495Tyr
NM_001387721.1:c.1483G>T	NP_001374650.1:p.Asp495Tyr
NM_005781.5:c.1483G>T	NP_005772.3:p.Asp495Tyr
NR_170678.1:n.1730G>T
NR_170679.1:n.2034G>T
NR_170680.1:n.1741G>T
NR_170681.1:n.1741G>T
NR_170682.1:n.2008G>T
NR_170683.1:n.2008G>T
NR_170684.1:n.1421G>T
NR_170685.1:n.1879G>T
NR_170686.1:n.1792G>T
NR_170687.1:n.1722G>T
NR_170688.1:n.2008G>T
NR_170689.1:n.1522G>T
NR_170690.1:n.1333G>T
NR_170691.1:n.1680G>T
NR_170692.1:n.1290G>T