Canonical Allele Identifier: CA2708985357
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs2111943157

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882021_56882023del , CM000667.2:g.56882021_56882023del GRCh38
NC_000005.9:g.56177848_56177850del , CM000667.1:g.56177848_56177850del GRCh37
NC_000005.8:g.56213605_56213607del NCBI36
NG_031884.1:g.71949_71951del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2821_2823del MANE Select ENSP00000382423.3:p.Ser941del
ENST00000399503.3:c.2821_2823del ENSP00000382423.3:p.Ser941del
NM_005921.1:c.2821_2823del NP_005912.1:p.Ser941del
XM_005248519.3:c.2443_2445del XP_005248576.2:p.Ser815del
XM_011543406.1:c.2566_2568del XP_011541708.1:p.Ser856del
XM_011543407.1:c.2542_2544del XP_011541709.1:p.Ser848del
XM_011543408.1:c.2821_2823del XP_011541710.1:p.Ser941del
XM_017009484.1:c.2410_2412del XP_016864973.1:p.Ser804del
XM_017009485.1:c.2332_2334del XP_016864974.1:p.Ser778del
XR_001742068.2:n.2852_2854del
NM_005921.2:c.2821_2823del MANE Select NP_005912.1:p.Ser941del