Canonical Allele Identifier: CA359802686
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs2111874713

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859898A>T , CM000667.2:g.56859898A>T GRCh38
NC_000005.9:g.56155725A>T , CM000667.1:g.56155725A>T GRCh37
NC_000005.8:g.56191482A>T NCBI36
NG_031884.1:g.49826A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.817A>T MANE Select ENSP00000382423.3:p.Arg273Ter
ENST00000399503.3:c.817A>T ENSP00000382423.3:p.Arg273Ter
NM_005921.1:c.817A>T NP_005912.1:p.Arg273Ter
XM_005248519.3:c.439A>T XP_005248576.2:p.Arg147Ter
XM_011543406.1:c.562A>T XP_011541708.1:p.Arg188Ter
XM_011543407.1:c.817A>T XP_011541709.1:p.Arg273Ter
XM_011543408.1:c.817A>T XP_011541710.1:p.Arg273Ter
XM_017009484.1:c.406A>T XP_016864973.1:p.Arg136Ter
XM_017009485.1:c.328A>T XP_016864974.1:p.Arg110Ter
XR_001742068.2:n.848A>T
NM_005921.2:c.817A>T MANE Select NP_005912.1:p.Arg273Ter