Canonical Allele Identifier: CA1548129157
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859668C= , CM000667.2:g.56859668C= GRCh38
NC_000005.9:g.56155495C= , CM000667.1:g.56155495C= GRCh37
NC_000005.8:g.56191252C= NCBI36
NG_031884.1:g.49596C=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.634-47C= MANE Select ENSP00000382423.3:n.634-47C=
ENST00000399503.3:c.634-47C= ENSP00000382423.3:n.634-47C=
NM_005921.1:c.634-47C= NP_005912.1:n.634-47C=
XM_005248519.3:c.256-47C= XP_005248576.2:n.256-47C=
XM_011543406.1:c.379-47C= XP_011541708.1:n.379-47C=
XM_011543407.1:c.634-47C= XP_011541709.1:n.634-47C=
XM_011543408.1:c.634-47C= XP_011541710.1:n.634-47C=
XM_017009484.1:c.223-47C= XP_016864973.1:n.223-47C=
XM_017009485.1:c.145-47C= XP_016864974.1:n.145-47C=
XR_001742068.2:n.665-47C=
NM_005921.2:c.634-47C= MANE Select NP_005912.1:n.634-47C=