Canonical Allele Identifier: CA437747023

Gene: TNK2

Linked Data

• MyVariant Identifiers: chr3:g.195597019G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.195870148G>A , CM000665.2:g.195870148G>A	GRCh38
NC_000003.11:g.195597019G>A , CM000665.1:g.195597019G>A	GRCh37
NC_000003.10:g.197081416G>A	NCBI36
NG_029779.1:g.43862C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000672887.2:c.1509C>T MANE Select	ENSP00000499899.1:p.Thr503=
ENST00000333602.14:c.1509C>T	ENSP00000329425.6:p.Thr503=
ENST00000381916.7:c.1698C>T	ENSP00000371341.2:p.Thr566=
ENST00000428187.7:c.1605C>T	ENSP00000392546.1:p.Thr535=
ENST00000439230.6:c.*121C>T	ENSP00000395588.1:n.*121C>T
ENST00000671753.1:c.1581C>T	ENSP00000499858.1:p.Thr527=
ENST00000671767.1:c.303C>T	ENSP00000499862.1:p.Thr101=
ENST00000672024.1:c.1509C>T	ENSP00000500486.1:p.Thr503=
ENST00000672098.1:c.39C>T	ENSP00000500684.1:p.Thr13=
ENST00000672320.1:n.359C>T
ENST00000672548.1:c.39C>T	ENSP00000500238.1:p.Thr13=
ENST00000672614.1:n.4017C>T
ENST00000672669.1:c.39C>T	ENSP00000500276.1:p.Thr13=
ENST00000672886.1:c.39C>T	ENSP00000500479.1:p.Thr13=
ENST00000672887.1:c.1509C>T	ENSP00000499899.1:p.Thr503=
ENST00000673038.1:c.1605C>T	ENSP00000500452.1:p.Thr535=
ENST00000673358.1:n.1106C>T
ENST00000673374.1:c.*484C>T	ENSP00000500225.1:n.*484C>T
ENST00000673420.1:c.1509C>T	ENSP00000500887.1:p.Thr503=
ENST00000673440.1:n.21C>T
ENST00000678220.1:c.1605C>T	ENSP00000503221.1:p.Thr535=
ENST00000333602.10:c.1509C>T	ENSP00000329425.6:p.Thr503=
ENST00000381916.6:c.1698C>T	ENSP00000371341.2:p.Thr566=
ENST00000411741.1:c.444C>T	ENSP00000415126.1:p.Thr148=
ENST00000416152.5:c.165C>T	ENSP00000398614.1:p.Thr55=
ENST00000424563.5:c.338C>T
ENST00000428187.5:c.1605C>T	ENSP00000392546.1:p.Thr535=
ENST00000439230.5:c.*121C>T	ENSP00000395588.1:n.*121C>T
ENST00000464041.5:n.1614C>T
ENST00000478623.5:n.327C>T
ENST00000478715.1:n.359C>T
ENST00000481865.5:n.4017C>T
ENST00000489628.1:n.1106C>T
ENST00000495247.5:n.21C>T
NM_001010938.1:c.1698C>T	NP_001010938.1:p.Thr566=
NM_001308046.1:c.1605C>T	NP_001294975.1:p.Thr535=
NM_005781.4:c.1509C>T	NP_005772.3:p.Thr503=
XM_005269268.3:c.1698C>T	XP_005269325.1:p.Thr566=
XM_005269270.3:c.1509C>T	XP_005269327.1:p.Thr503=
XM_005269274.3:c.792C>T	XP_005269331.1:p.Thr264=
XM_005269275.3:c.567C>T	XP_005269332.1:p.Thr189=
XM_011512317.1:c.2001C>T	XP_011510619.1:p.Thr667=
XM_011512318.1:c.1509C>T	XP_011510620.1:p.Thr503=
XM_011512319.1:c.1509C>T	XP_011510621.1:p.Thr503=
XM_011512320.1:c.1509C>T	XP_011510622.1:p.Thr503=
XM_011512321.1:c.1281C>T	XP_011510623.1:p.Thr427=
XM_011512317.3:c.2001C>T	XP_011510619.1:p.Thr667=
XM_011512318.2:c.1605C>T	XP_011510620.2:p.Thr535=
XM_011512321.2:c.1281C>T	XP_011510623.1:p.Thr427=
XM_017005508.1:c.1605C>T	XP_016860997.1:p.Thr535=
XM_017005509.1:c.1605C>T	XP_016860998.1:p.Thr535=
XM_017005510.1:c.1605C>T	XP_016860999.1:p.Thr535=
XM_024453291.1:c.1701C>T	XP_024309059.1:p.Thr567=
XM_024453292.1:c.1560C>T	XP_024309060.1:p.Thr520=
XM_024453293.1:c.1509C>T	XP_024309061.1:p.Thr503=
XM_024453294.1:c.1509C>T	XP_024309062.1:p.Thr503=
XM_024453295.1:c.1509C>T	XP_024309063.1:p.Thr503=
NM_001010938.2:c.1581C>T	NP_001010938.2:p.Thr527=
NM_001308046.2:c.1605C>T	NP_001294975.1:p.Thr535=
NM_001382271.1:c.1605C>T	NP_001369200.1:p.Thr535=
NM_001382272.1:c.1581C>T	NP_001369201.1:p.Thr527=
NM_001382273.1:c.1509C>T MANE Select	NP_001369202.1:p.Thr503=
NM_001382274.1:c.1509C>T	NP_001369203.1:p.Thr503=
NM_001382275.1:c.1605C>T	NP_001369204.1:p.Thr535=
NM_001386164.1:c.1509C>T	NP_001373093.1:p.Thr503=
NM_001387707.1:c.1605C>T	NP_001374636.1:p.Thr535=
NM_001387708.1:c.1581C>T	NP_001374637.1:p.Thr527=
NM_001387709.1:c.1509C>T	NP_001374638.1:p.Thr503=
NM_001387710.1:c.1509C>T	NP_001374639.1:p.Thr503=
NM_001387711.1:c.1509C>T	NP_001374640.1:p.Thr503=
NM_001387712.1:c.1509C>T	NP_001374641.1:p.Thr503=
NM_001387713.1:c.1509C>T	NP_001374642.1:p.Thr503=
NM_001387714.1:c.1509C>T	NP_001374643.1:p.Thr503=
NM_001387715.1:c.1581C>T	NP_001374644.1:p.Thr527=
NM_001387716.1:c.1509C>T	NP_001374645.1:p.Thr503=
NM_001387717.1:c.1509C>T	NP_001374646.1:p.Thr503=
NM_001387718.1:c.1509C>T	NP_001374647.1:p.Thr503=
NM_001387719.1:c.1509C>T	NP_001374648.1:p.Thr503=
NM_001387720.1:c.1509C>T	NP_001374649.1:p.Thr503=
NM_001387721.1:c.1509C>T	NP_001374650.1:p.Thr503=
NM_005781.5:c.1509C>T	NP_005772.3:p.Thr503=
NR_170678.1:n.1756C>T
NR_170679.1:n.2060C>T
NR_170680.1:n.1767C>T
NR_170681.1:n.1767C>T
NR_170682.1:n.2034C>T
NR_170683.1:n.2034C>T
NR_170684.1:n.1447C>T
NR_170685.1:n.1905C>T
NR_170686.1:n.1818C>T
NR_170687.1:n.1748C>T
NR_170688.1:n.2034C>T
NR_170689.1:n.1548C>T
NR_170690.1:n.1359C>T
NR_170691.1:n.1706C>T
NR_170692.1:n.1316C>T