Canonical Allele Identifier: CA917480357
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs869198967

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882033del , CM000667.2:g.56882033del GRCh38
NC_000005.9:g.56177860del , CM000667.1:g.56177860del GRCh37
NC_000005.8:g.56213617del NCBI36
NG_031884.1:g.71961del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2833del MANE Select ENSP00000382423.3:p.Thr945GlnfsTer23
ENST00000399503.3:c.2833del ENSP00000382423.3:p.Thr945GlnfsTer23
NM_005921.1:c.2833del NP_005912.1:p.Thr945GlnfsTer23
XM_005248519.3:c.2455del XP_005248576.2:p.Thr819GlnfsTer23
XM_011543406.1:c.2578del XP_011541708.1:p.Thr860GlnfsTer23
XM_011543407.1:c.2554del XP_011541709.1:p.Thr852GlnfsTer23
XM_011543408.1:c.2833del XP_011541710.1:p.Thr945GlnfsTer23
XM_017009484.1:c.2422del XP_016864973.1:p.Thr808GlnfsTer23
XM_017009485.1:c.2344del XP_016864974.1:p.Thr782GlnfsTer23
XR_001742068.2:n.2864del
NM_005921.2:c.2833del MANE Select NP_005912.1:p.Thr945GlnfsTer23