Canonical Allele Identifier: CA1548139354
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881902C= , CM000667.2:g.56881902C= GRCh38
NC_000005.9:g.56177729C= , CM000667.1:g.56177729C= GRCh37
NC_000005.8:g.56213486C= NCBI36
NG_031884.1:g.71830C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2702C= MANE Select ENSP00000382423.3:p.Ser901=
ENST00000399503.3:c.2702C= ENSP00000382423.3:p.Ser901=
NM_005921.1:c.2702C= NP_005912.1:p.Ser901=
XM_005248519.3:c.2324C= XP_005248576.2:p.Ser775=
XM_011543406.1:c.2447C= XP_011541708.1:p.Ser816=
XM_011543407.1:c.2423C= XP_011541709.1:p.Ser808=
XM_011543408.1:c.2702C= XP_011541710.1:p.Ser901=
XM_017009484.1:c.2291C= XP_016864973.1:p.Ser764=
XM_017009485.1:c.2213C= XP_016864974.1:p.Ser738=
XR_001742068.2:n.2733C=
NM_005921.2:c.2702C= MANE Select NP_005912.1:p.Ser901=