Canonical Allele Identifier: CA1548129310
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56860008C= , CM000667.2:g.56860008C= GRCh38
NC_000005.9:g.56155835C= , CM000667.1:g.56155835C= GRCh37
NC_000005.8:g.56191592C= NCBI36
NG_031884.1:g.49936C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.834+93C= MANE Select ENSP00000382423.3:n.834+93C=
ENST00000399503.3:c.834+93C= ENSP00000382423.3:n.834+93C=
NM_005921.1:c.834+93C= NP_005912.1:n.834+93C=
XM_005248519.3:c.456+93C= XP_005248576.2:n.456+93C=
XM_011543406.1:c.579+93C= XP_011541708.1:n.579+93C=
XM_011543407.1:c.834+93C= XP_011541709.1:n.834+93C=
XM_011543408.1:c.834+93C= XP_011541710.1:n.834+93C=
XM_017009484.1:c.423+93C= XP_016864973.1:n.423+93C=
XM_017009485.1:c.345+93C= XP_016864974.1:n.345+93C=
XR_001742068.2:n.865+93C=
NM_005921.2:c.834+93C= MANE Select NP_005912.1:n.834+93C=