Canonical Allele Identifier: CA1548139445
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882084C= , CM000667.2:g.56882084C= GRCh38
NC_000005.9:g.56177911C= , CM000667.1:g.56177911C= GRCh37
NC_000005.8:g.56213668C= NCBI36
NG_031884.1:g.72012C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2884C= MANE Select ENSP00000382423.3:p.Pro962=
ENST00000399503.3:c.2884C= ENSP00000382423.3:p.Pro962=
NM_005921.1:c.2884C= NP_005912.1:p.Pro962=
XM_005248519.3:c.2506C= XP_005248576.2:p.Pro836=
XM_011543406.1:c.2629C= XP_011541708.1:p.Pro877=
XM_011543407.1:c.2605C= XP_011541709.1:p.Pro869=
XM_011543408.1:c.2884C= XP_011541710.1:p.Pro962=
XM_017009484.1:c.2473C= XP_016864973.1:p.Pro825=
XM_017009485.1:c.2395C= XP_016864974.1:p.Pro799=
XR_001742068.2:n.2915C=
NM_005921.2:c.2884C= MANE Select NP_005912.1:p.Pro962=