Canonical Allele Identifier: CA1548136438
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875204G= , CM000667.2:g.56875204G= GRCh38
NC_000005.9:g.56171031G= , CM000667.1:g.56171031G= GRCh37
NC_000005.8:g.56206788G= NCBI36
NG_031884.1:g.65132G=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.1859G= MANE Select ENSP00000382423.3:p.Ser620=
ENST00000399503.3:c.1859G= ENSP00000382423.3:p.Ser620=
NM_005921.1:c.1859G= NP_005912.1:p.Ser620=
XM_005248519.3:c.1481G= XP_005248576.2:p.Ser494=
XM_011543406.1:c.1604G= XP_011541708.1:p.Ser535=
XM_011543407.1:c.1686+2199G= XP_011541709.1:n.1686+2199G=
XM_011543408.1:c.1859G= XP_011541710.1:p.Ser620=
XM_017009484.1:c.1448G= XP_016864973.1:p.Ser483=
XM_017009485.1:c.1370G= XP_016864974.1:p.Ser457=
XR_001742068.2:n.1890G=
NM_005921.2:c.1859G= MANE Select NP_005912.1:p.Ser620=