Canonical Allele Identifier: CA1548139581
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882394C= , CM000667.2:g.56882394C= GRCh38
NC_000005.9:g.56178221C= , CM000667.1:g.56178221C= GRCh37
NC_000005.8:g.56213978C= NCBI36
NG_031884.1:g.72322C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3194C= MANE Select ENSP00000382423.3:p.Pro1065=
ENST00000399503.3:c.3194C= ENSP00000382423.3:p.Pro1065=
NM_005921.1:c.3194C= NP_005912.1:p.Pro1065=
XM_005248519.3:c.2816C= XP_005248576.2:p.Pro939=
XM_011543406.1:c.2939C= XP_011541708.1:p.Pro980=
XM_011543407.1:c.2915C= XP_011541709.1:p.Pro972=
XM_011543408.1:c.3194C= XP_011541710.1:p.Pro1065=
XM_017009484.1:c.2783C= XP_016864973.1:p.Pro928=
XM_017009485.1:c.2705C= XP_016864974.1:p.Pro902=
XR_001742068.2:n.3225C=
NM_005921.2:c.3194C= MANE Select NP_005912.1:p.Pro1065=