Canonical Allele Identifier: CA1548129186
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859736A= , CM000667.2:g.56859736A= GRCh38
NC_000005.9:g.56155563A= , CM000667.1:g.56155563A= GRCh37
NC_000005.8:g.56191320A= NCBI36
NG_031884.1:g.49664A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.655A= MANE Select ENSP00000382423.3:p.Lys219=
ENST00000399503.3:c.655A= ENSP00000382423.3:p.Lys219=
NM_005921.1:c.655A= NP_005912.1:p.Lys219=
XM_005248519.3:c.277A= XP_005248576.2:p.Lys93=
XM_011543406.1:c.400A= XP_011541708.1:p.Lys134=
XM_011543407.1:c.655A= XP_011541709.1:p.Lys219=
XM_011543408.1:c.655A= XP_011541710.1:p.Lys219=
XM_017009484.1:c.244A= XP_016864973.1:p.Lys82=
XM_017009485.1:c.166A= XP_016864974.1:p.Lys56=
XR_001742068.2:n.686A=
NM_005921.2:c.655A= MANE Select NP_005912.1:p.Lys219=