Canonical Allele Identifier: CA2776321

Gene: TNK2

Linked Data

• ClinVar Variation Id: 2871677
• ClinVar RCV Id: RCV003698635
• dbSNP Id: rs35759128
• ExAC: 3:195597009 G / A
• gnomAD v2: 3-195597009-G-A
• gnomAD v3: 3-195870138-G-A
• gnomAD v4: 3-195870138-G-A
• MyVariant Identifiers: chr3:g.195597009G>A (hg19) ; chr3:g.195870138G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.195870138G>A , CM000665.2:g.195870138G>A	GRCh38
NC_000003.11:g.195597009G>A , CM000665.1:g.195597009G>A	GRCh37
NC_000003.10:g.197081406G>A	NCBI36
NG_029779.1:g.43872C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000672887.2:c.1519C>T MANE Select	ENSP00000499899.1:p.Pro507Ser
ENST00000333602.14:c.1519C>T	ENSP00000329425.6:p.Pro507Ser
ENST00000381916.7:c.1708C>T	ENSP00000371341.2:p.Pro570Ser
ENST00000428187.7:c.1615C>T	ENSP00000392546.1:p.Pro539Ser
ENST00000439230.6:c.*131C>T	ENSP00000395588.1:n.*131C>T
ENST00000671753.1:c.1591C>T	ENSP00000499858.1:p.Pro531Ser
ENST00000671767.1:c.313C>T	ENSP00000499862.1:p.Pro105Ser
ENST00000672024.1:c.1519C>T	ENSP00000500486.1:p.Pro507Ser
ENST00000672098.1:c.49C>T	ENSP00000500684.1:p.Pro17Ser
ENST00000672320.1:n.369C>T
ENST00000672548.1:c.49C>T	ENSP00000500238.1:p.Pro17Ser
ENST00000672614.1:n.4027C>T
ENST00000672669.1:c.49C>T	ENSP00000500276.1:p.Pro17Ser
ENST00000672886.1:c.49C>T	ENSP00000500479.1:p.Pro17Ser
ENST00000672887.1:c.1519C>T	ENSP00000499899.1:p.Pro507Ser
ENST00000673038.1:c.1615C>T	ENSP00000500452.1:p.Pro539Ser
ENST00000673358.1:n.1116C>T
ENST00000673374.1:c.*494C>T	ENSP00000500225.1:n.*494C>T
ENST00000673420.1:c.1519C>T	ENSP00000500887.1:p.Pro507Ser
ENST00000673440.1:n.31C>T
ENST00000678220.1:c.1615C>T	ENSP00000503221.1:p.Pro539Ser
ENST00000333602.10:c.1519C>T	ENSP00000329425.6:p.Pro507Ser
ENST00000381916.6:c.1708C>T	ENSP00000371341.2:p.Pro570Ser
ENST00000411741.1:c.454C>T	ENSP00000415126.1:p.Pro152Ser
ENST00000416152.5:c.175C>T	ENSP00000398614.1:p.Pro59Ser
ENST00000424563.5:c.348C>T
ENST00000428187.5:c.1615C>T	ENSP00000392546.1:p.Pro539Ser
ENST00000439230.5:c.*131C>T	ENSP00000395588.1:n.*131C>T
ENST00000464041.5:n.1624C>T
ENST00000478623.5:n.337C>T
ENST00000478715.1:n.369C>T
ENST00000481865.5:n.4027C>T
ENST00000489628.1:n.1116C>T
ENST00000495247.5:n.31C>T
NM_001010938.1:c.1708C>T	NP_001010938.1:p.Pro570Ser
NM_001308046.1:c.1615C>T	NP_001294975.1:p.Pro539Ser
NM_005781.4:c.1519C>T	NP_005772.3:p.Pro507Ser
XM_005269268.3:c.1708C>T	XP_005269325.1:p.Pro570Ser
XM_005269270.3:c.1519C>T	XP_005269327.1:p.Pro507Ser
XM_005269274.3:c.802C>T	XP_005269331.1:p.Pro268Ser
XM_005269275.3:c.577C>T	XP_005269332.1:p.Pro193Ser
XM_011512317.1:c.2011C>T	XP_011510619.1:p.Pro671Ser
XM_011512318.1:c.1519C>T	XP_011510620.1:p.Pro507Ser
XM_011512319.1:c.1519C>T	XP_011510621.1:p.Pro507Ser
XM_011512320.1:c.1519C>T	XP_011510622.1:p.Pro507Ser
XM_011512321.1:c.1291C>T	XP_011510623.1:p.Pro431Ser
XM_011512317.3:c.2011C>T	XP_011510619.1:p.Pro671Ser
XM_011512318.2:c.1615C>T	XP_011510620.2:p.Pro539Ser
XM_011512321.2:c.1291C>T	XP_011510623.1:p.Pro431Ser
XM_017005508.1:c.1615C>T	XP_016860997.1:p.Pro539Ser
XM_017005509.1:c.1615C>T	XP_016860998.1:p.Pro539Ser
XM_017005510.1:c.1615C>T	XP_016860999.1:p.Pro539Ser
XM_024453291.1:c.1711C>T	XP_024309059.1:p.Pro571Ser
XM_024453292.1:c.1570C>T	XP_024309060.1:p.Pro524Ser
XM_024453293.1:c.1519C>T	XP_024309061.1:p.Pro507Ser
XM_024453294.1:c.1519C>T	XP_024309062.1:p.Pro507Ser
XM_024453295.1:c.1519C>T	XP_024309063.1:p.Pro507Ser
NM_001010938.2:c.1591C>T	NP_001010938.2:p.Pro531Ser
NM_001308046.2:c.1615C>T	NP_001294975.1:p.Pro539Ser
NM_001382271.1:c.1615C>T	NP_001369200.1:p.Pro539Ser
NM_001382272.1:c.1591C>T	NP_001369201.1:p.Pro531Ser
NM_001382273.1:c.1519C>T MANE Select	NP_001369202.1:p.Pro507Ser
NM_001382274.1:c.1519C>T	NP_001369203.1:p.Pro507Ser
NM_001382275.1:c.1615C>T	NP_001369204.1:p.Pro539Ser
NM_001386164.1:c.1519C>T	NP_001373093.1:p.Pro507Ser
NM_001387707.1:c.1615C>T	NP_001374636.1:p.Pro539Ser
NM_001387708.1:c.1591C>T	NP_001374637.1:p.Pro531Ser
NM_001387709.1:c.1519C>T	NP_001374638.1:p.Pro507Ser
NM_001387710.1:c.1519C>T	NP_001374639.1:p.Pro507Ser
NM_001387711.1:c.1519C>T	NP_001374640.1:p.Pro507Ser
NM_001387712.1:c.1519C>T	NP_001374641.1:p.Pro507Ser
NM_001387713.1:c.1519C>T	NP_001374642.1:p.Pro507Ser
NM_001387714.1:c.1519C>T	NP_001374643.1:p.Pro507Ser
NM_001387715.1:c.1591C>T	NP_001374644.1:p.Pro531Ser
NM_001387716.1:c.1519C>T	NP_001374645.1:p.Pro507Ser
NM_001387717.1:c.1519C>T	NP_001374646.1:p.Pro507Ser
NM_001387718.1:c.1519C>T	NP_001374647.1:p.Pro507Ser
NM_001387719.1:c.1519C>T	NP_001374648.1:p.Pro507Ser
NM_001387720.1:c.1519C>T	NP_001374649.1:p.Pro507Ser
NM_001387721.1:c.1519C>T	NP_001374650.1:p.Pro507Ser
NM_005781.5:c.1519C>T	NP_005772.3:p.Pro507Ser
NR_170678.1:n.1766C>T
NR_170679.1:n.2070C>T
NR_170680.1:n.1777C>T
NR_170681.1:n.1777C>T
NR_170682.1:n.2044C>T
NR_170683.1:n.2044C>T
NR_170684.1:n.1457C>T
NR_170685.1:n.1915C>T
NR_170686.1:n.1828C>T
NR_170687.1:n.1758C>T
NR_170688.1:n.2044C>T
NR_170689.1:n.1558C>T
NR_170690.1:n.1369C>T
NR_170691.1:n.1716C>T
NR_170692.1:n.1326C>T