Canonical Allele Identifier: CA359787699
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882319A>T , CM000667.2:g.56882319A>T GRCh38
NC_000005.9:g.56178146A>T , CM000667.1:g.56178146A>T GRCh37
NC_000005.8:g.56213903A>T NCBI36
NG_031884.1:g.72247A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3119A>T MANE Select ENSP00000382423.3:p.Asp1040Val
ENST00000399503.3:c.3119A>T ENSP00000382423.3:p.Asp1040Val
NM_005921.1:c.3119A>T NP_005912.1:p.Asp1040Val
XM_005248519.3:c.2741A>T XP_005248576.2:p.Asp914Val
XM_011543406.1:c.2864A>T XP_011541708.1:p.Asp955Val
XM_011543407.1:c.2840A>T XP_011541709.1:p.Asp947Val
XM_011543408.1:c.3119A>T XP_011541710.1:p.Asp1040Val
XM_017009484.1:c.2708A>T XP_016864973.1:p.Asp903Val
XM_017009485.1:c.2630A>T XP_016864974.1:p.Asp877Val
XR_001742068.2:n.3150A>T
NM_005921.2:c.3119A>T MANE Select NP_005912.1:p.Asp1040Val