Canonical Allele Identifier: CA645557008
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881738del , CM000667.2:g.56881738del GRCh38
NC_000005.9:g.56177565del , CM000667.1:g.56177565del GRCh37
NC_000005.8:g.56213322del NCBI36
NG_031884.1:g.71666del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2538del MANE Select ENSP00000382423.3:p.Thr847LeufsTer10
ENST00000399503.3:c.2538del ENSP00000382423.3:p.Thr847LeufsTer10
NM_005921.1:c.2538del NP_005912.1:p.Thr847LeufsTer10
XM_005248519.3:c.2160del XP_005248576.2:p.Thr721LeufsTer10
XM_011543406.1:c.2283del XP_011541708.1:p.Thr762LeufsTer10
XM_011543407.1:c.2259del XP_011541709.1:p.Thr754LeufsTer10
XM_011543408.1:c.2538del XP_011541710.1:p.Thr847LeufsTer10
XM_017009484.1:c.2127del XP_016864973.1:p.Thr710LeufsTer10
XM_017009485.1:c.2049del XP_016864974.1:p.Thr684LeufsTer10
XR_001742068.2:n.2569del
NM_005921.2:c.2538del MANE Select NP_005912.1:p.Thr847LeufsTer10