Canonical Allele Identifier: CA1548129214
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859801G= , CM000667.2:g.56859801G= GRCh38
NC_000005.9:g.56155628G= , CM000667.1:g.56155628G= GRCh37
NC_000005.8:g.56191385G= NCBI36
NG_031884.1:g.49729G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.720G= MANE Select ENSP00000382423.3:p.Ala240=
ENST00000399503.3:c.720G= ENSP00000382423.3:p.Ala240=
NM_005921.1:c.720G= NP_005912.1:p.Ala240=
XM_005248519.3:c.342G= XP_005248576.2:p.Ala114=
XM_011543406.1:c.465G= XP_011541708.1:p.Ala155=
XM_011543407.1:c.720G= XP_011541709.1:p.Ala240=
XM_011543408.1:c.720G= XP_011541710.1:p.Ala240=
XM_017009484.1:c.309G= XP_016864973.1:p.Ala103=
XM_017009485.1:c.231G= XP_016864974.1:p.Ala77=
XR_001742068.2:n.751G=
NM_005921.2:c.720G= MANE Select NP_005912.1:p.Ala240=