Canonical Allele Identifier: CA1548136437
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875203A= , CM000667.2:g.56875203A= GRCh38
NC_000005.9:g.56171030A= , CM000667.1:g.56171030A= GRCh37
NC_000005.8:g.56206787A= NCBI36
NG_031884.1:g.65131A=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.1858A= MANE Select ENSP00000382423.3:p.Ser620=
ENST00000399503.3:c.1858A= ENSP00000382423.3:p.Ser620=
NM_005921.1:c.1858A= NP_005912.1:p.Ser620=
XM_005248519.3:c.1480A= XP_005248576.2:p.Ser494=
XM_011543406.1:c.1603A= XP_011541708.1:p.Ser535=
XM_011543407.1:c.1686+2198A= XP_011541709.1:n.1686+2198A=
XM_011543408.1:c.1858A= XP_011541710.1:p.Ser620=
XM_017009484.1:c.1447A= XP_016864973.1:p.Ser483=
XM_017009485.1:c.1369A= XP_016864974.1:p.Ser457=
XR_001742068.2:n.1889A=
NM_005921.2:c.1858A= MANE Select NP_005912.1:p.Ser620=