Canonical Allele Identifier: CA359802473
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs55694258

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859791A>T , CM000667.2:g.56859791A>T GRCh38
NC_000005.9:g.56155618A>T , CM000667.1:g.56155618A>T GRCh37
NC_000005.8:g.56191375A>T NCBI36
NG_031884.1:g.49719A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.710A>T MANE Select ENSP00000382423.3:p.Gln237Leu
ENST00000399503.3:c.710A>T ENSP00000382423.3:p.Gln237Leu
NM_005921.1:c.710A>T NP_005912.1:p.Gln237Leu
XM_005248519.3:c.332A>T XP_005248576.2:p.Gln111Leu
XM_011543406.1:c.455A>T XP_011541708.1:p.Gln152Leu
XM_011543407.1:c.710A>T XP_011541709.1:p.Gln237Leu
XM_011543408.1:c.710A>T XP_011541710.1:p.Gln237Leu
XM_017009484.1:c.299A>T XP_016864973.1:p.Gln100Leu
XM_017009485.1:c.221A>T XP_016864974.1:p.Gln74Leu
XR_001742068.2:n.741A>T
NM_005921.2:c.710A>T MANE Select NP_005912.1:p.Gln237Leu