Canonical Allele Identifier: CA1548136427
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875182A= , CM000667.2:g.56875182A= GRCh38
NC_000005.9:g.56171009A= , CM000667.1:g.56171009A= GRCh37
NC_000005.8:g.56206766A= NCBI36
NG_031884.1:g.65110A=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.1837A= MANE Select ENSP00000382423.3:p.Ser613=
ENST00000399503.3:c.1837A= ENSP00000382423.3:p.Ser613=
NM_005921.1:c.1837A= NP_005912.1:p.Ser613=
XM_005248519.3:c.1459A= XP_005248576.2:p.Ser487=
XM_011543406.1:c.1582A= XP_011541708.1:p.Ser528=
XM_011543407.1:c.1686+2177A= XP_011541709.1:n.1686+2177A=
XM_011543408.1:c.1837A= XP_011541710.1:p.Ser613=
XM_017009484.1:c.1426A= XP_016864973.1:p.Ser476=
XM_017009485.1:c.1348A= XP_016864974.1:p.Ser450=
XR_001742068.2:n.1868A=
NM_005921.2:c.1837A= MANE Select NP_005912.1:p.Ser613=