Canonical Allele Identifier: CA1548129207
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859789C= , CM000667.2:g.56859789C= GRCh38
NC_000005.9:g.56155616C= , CM000667.1:g.56155616C= GRCh37
NC_000005.8:g.56191373C= NCBI36
NG_031884.1:g.49717C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.708C= MANE Select ENSP00000382423.3:p.Val236=
ENST00000399503.3:c.708C= ENSP00000382423.3:p.Val236=
NM_005921.1:c.708C= NP_005912.1:p.Val236=
XM_005248519.3:c.330C= XP_005248576.2:p.Val110=
XM_011543406.1:c.453C= XP_011541708.1:p.Val151=
XM_011543407.1:c.708C= XP_011541709.1:p.Val236=
XM_011543408.1:c.708C= XP_011541710.1:p.Val236=
XM_017009484.1:c.297C= XP_016864973.1:p.Val99=
XM_017009485.1:c.219C= XP_016864974.1:p.Val73=
XR_001742068.2:n.739C=
NM_005921.2:c.708C= MANE Select NP_005912.1:p.Val236=