Canonical Allele Identifier: CA359802522
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs1579753824
gnomAD v3: 5-56859817-A-G
gnomAD v4: 5-56859817-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859817A>G , CM000667.2:g.56859817A>G GRCh38
NC_000005.9:g.56155644A>G , CM000667.1:g.56155644A>G GRCh37
NC_000005.8:g.56191401A>G NCBI36
NG_031884.1:g.49745A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.736A>G MANE Select ENSP00000382423.3:p.Lys246Glu
ENST00000399503.3:c.736A>G ENSP00000382423.3:p.Lys246Glu
NM_005921.1:c.736A>G NP_005912.1:p.Lys246Glu
XM_005248519.3:c.358A>G XP_005248576.2:p.Lys120Glu
XM_011543406.1:c.481A>G XP_011541708.1:p.Lys161Glu
XM_011543407.1:c.736A>G XP_011541709.1:p.Lys246Glu
XM_011543408.1:c.736A>G XP_011541710.1:p.Lys246Glu
XM_017009484.1:c.325A>G XP_016864973.1:p.Lys109Glu
XM_017009485.1:c.247A>G XP_016864974.1:p.Lys83Glu
XR_001742068.2:n.767A>G
NM_005921.2:c.736A>G MANE Select NP_005912.1:p.Lys246Glu