Canonical Allele Identifier: CA3109738968
Community Standard Title: NM_001382273.1(TNK2):c.3108C= (p.Asn1036=)
Gene: TNK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.195866942G= , CM000665.2:g.195866942G= GRCh38
NC_000003.11:g.195593813G= , CM000665.1:g.195593813G= GRCh37
NC_000003.10:g.197078210G= NCBI36
NG_029779.1:g.47068C=

Transcript Alleles

HGVS Amino-acid Change
NM_001382273.1:c.3108C= MANE Select NP_001369202.1:p.Asn1036=
ENST00000672887.2:c.3108C= MANE Select ENSP00000499899.1:p.Asn1036=
NM_001010938.1:c.3201C= NP_001010938.1:p.Asn1067=
NM_001010938.2:c.3084C= NP_001010938.2:p.Asn1028=
NM_001308046.1:c.3063C= NP_001294975.1:p.Asn1021=
NM_001308046.2:c.3063C= NP_001294975.1:p.Asn1021=
NM_001382271.1:c.3159C= NP_001369200.1:p.Asn1053=
NM_001382272.1:c.3180C= NP_001369201.1:p.Asn1060=
NM_001382274.1:c.3108C= NP_001369203.1:p.Asn1036=
NM_001382275.1:c.3108C= NP_001369204.1:p.Asn1036=
NM_001386164.1:c.3063C= NP_001373093.1:p.Asn1021=
NM_001387707.1:c.3204C= NP_001374636.1:p.Asn1068=
NM_001387708.1:c.3135C= NP_001374637.1:p.Asn1045=
NM_001387709.1:c.3063C= NP_001374638.1:p.Asn1021=
NM_001387710.1:c.3063C= NP_001374639.1:p.Asn1021=
NM_001387711.1:c.3063C= NP_001374640.1:p.Asn1021=
NM_001387712.1:c.3063C= NP_001374641.1:p.Asn1021=
NM_001387713.1:c.3057C= NP_001374642.1:p.Asn1019=
NM_001387714.1:c.3057C= NP_001374643.1:p.Asn1019=
NM_001387715.1:c.3039C= NP_001374644.1:p.Asn1013=
NM_001387716.1:c.3012C= NP_001374645.1:p.Asn1004=
NM_001387717.1:c.3012C= NP_001374646.1:p.Asn1004=
NM_001387718.1:c.3012C= NP_001374647.1:p.Asn1004=
NM_001387719.1:c.2967C= NP_001374648.1:p.Asn989=
NM_001387720.1:c.2967C= NP_001374649.1:p.Asn989=
NM_001387721.1:c.2967C= NP_001374650.1:p.Asn989=
NM_005781.4:c.3057C= NP_005772.3:p.Asn1019=
NM_005781.5:c.3057C= NP_005772.3:p.Asn1019=
NR_170678.1:n.3355C=
NR_170679.1:n.3659C=
NR_170680.1:n.3366C=
NR_170681.1:n.3321C=
NR_170682.1:n.3633C=
NR_170683.1:n.3588C=
NR_170684.1:n.3001C=
NR_170685.1:n.3504C=
NR_170686.1:n.3372C=
NR_170687.1:n.3341C=
NR_170688.1:n.3582C=
NR_170689.1:n.3102C=
NR_170690.1:n.2907C=
NR_170691.1:n.3260C=
NR_170692.1:n.2870C=
ENST00000333602.10:c.3057C= ENSP00000329425.6:p.Asn1019=
ENST00000333602.14:c.3057C= ENSP00000329425.6:p.Asn1019=
ENST00000381916.6:c.3201C= ENSP00000371341.2:p.Asn1067=
ENST00000381916.7:c.3201C= ENSP00000371341.2:p.Asn1067=
ENST00000416152.5:c.1764C= ENSP00000398614.1:p.Asn588=
ENST00000420716.2:n.2501C=
ENST00000428187.5:c.3063C= ENSP00000392546.1:p.Asn1021=
ENST00000428187.7:c.3063C= ENSP00000392546.1:p.Asn1021=
ENST00000671753.1:c.3084C= ENSP00000499858.1:p.Asn1028=
ENST00000672024.1:c.2967C= ENSP00000500486.1:p.Asn989=
ENST00000672548.1:c.1593C= ENSP00000500238.1:p.Asn531=
ENST00000672887.1:c.3108C= ENSP00000499899.1:p.Asn1036=
ENST00000673038.1:c.3159C= ENSP00000500452.1:p.Asn1053=
ENST00000673236.1:n.2501C=
ENST00000673420.1:c.3063C= ENSP00000500887.1:p.Asn1021=
ENST00000678220.1:c.3159C= ENSP00000503221.1:p.Asn1053=
XM_005269268.3:c.3297C= XP_005269325.1:p.Asn1099=
XM_005269270.3:c.3108C= XP_005269327.1:p.Asn1036=
XM_005269274.3:c.2391C= XP_005269331.1:p.Asn797=
XM_005269275.3:c.2166C= XP_005269332.1:p.Asn722=
XM_011512317.1:c.3600C= XP_011510619.1:p.Asn1200=
XM_011512317.3:c.3600C= XP_011510619.1:p.Asn1200=
XM_011512318.1:c.3102C= XP_011510620.1:p.Asn1034=
XM_011512318.2:c.3198C= XP_011510620.2:p.Asn1066=
XM_011512319.1:c.3063C= XP_011510621.1:p.Asn1021=
XM_011512320.1:c.3108C= XP_011510622.1:p.Asn1036=
XM_011512321.1:c.2880C= XP_011510623.1:p.Asn960=
XM_011512321.2:c.2880C= XP_011510623.1:p.Asn960=
XM_017005508.1:c.3159C= XP_016860997.1:p.Asn1053=
XM_017005509.1:c.3153C= XP_016860998.1:p.Asn1051=
XM_017005510.1:c.3108C= XP_016860999.1:p.Asn1036=
XM_024453291.1:c.3300C= XP_024309059.1:p.Asn1100=
XM_024453292.1:c.3159C= XP_024309060.1:p.Asn1053=
XM_024453293.1:c.3108C= XP_024309061.1:p.Asn1036=
XM_024453294.1:c.3108C= XP_024309062.1:p.Asn1036=
XM_024453295.1:c.3108C= XP_024309063.1:p.Asn1036=