Canonical Allele Identifier: CA1548139321
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881817G= , CM000667.2:g.56881817G= GRCh38
NC_000005.9:g.56177644G= , CM000667.1:g.56177644G= GRCh37
NC_000005.8:g.56213401G= NCBI36
NG_031884.1:g.71745G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2617G= MANE Select ENSP00000382423.3:p.Val873=
ENST00000399503.3:c.2617G= ENSP00000382423.3:p.Val873=
NM_005921.1:c.2617G= NP_005912.1:p.Val873=
XM_005248519.3:c.2239G= XP_005248576.2:p.Val747=
XM_011543406.1:c.2362G= XP_011541708.1:p.Val788=
XM_011543407.1:c.2338G= XP_011541709.1:p.Val780=
XM_011543408.1:c.2617G= XP_011541710.1:p.Val873=
XM_017009484.1:c.2206G= XP_016864973.1:p.Val736=
XM_017009485.1:c.2128G= XP_016864974.1:p.Val710=
XR_001742068.2:n.2648G=
NM_005921.2:c.2617G= MANE Select NP_005912.1:p.Val873=