Canonical Allele Identifier: CA1548129241
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs1747452409

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859857_56859865del , CM000667.2:g.56859857_56859865del GRCh38
NC_000005.9:g.56155684_56155692del , CM000667.1:g.56155684_56155692del GRCh37
NC_000005.8:g.56191441_56191449del NCBI36
NG_031884.1:g.49785_49793del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.776_784del MANE Select ENSP00000382423.3:p.Gly259_Thr261del
ENST00000399503.3:c.776_784del ENSP00000382423.3:p.Gly259_Thr261del
NM_005921.1:c.776_784del NP_005912.1:p.Gly259_Thr261del
XM_005248519.3:c.398_406del XP_005248576.2:p.Gly133_Thr135del
XM_011543406.1:c.521_529del XP_011541708.1:p.Gly174_Thr176del
XM_011543407.1:c.776_784del XP_011541709.1:p.Gly259_Thr261del
XM_011543408.1:c.776_784del XP_011541710.1:p.Gly259_Thr261del
XM_017009484.1:c.365_373del XP_016864973.1:p.Gly122_Thr124del
XM_017009485.1:c.287_295del XP_016864974.1:p.Gly96_Thr98del
XR_001742068.2:n.807_815del
NM_005921.2:c.776_784del MANE Select NP_005912.1:p.Gly259_Thr261del