Canonical Allele Identifier: CA2708987437
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs2111944903

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882233del , CM000667.2:g.56882233del GRCh38
NC_000005.9:g.56178060del , CM000667.1:g.56178060del GRCh37
NC_000005.8:g.56213817del NCBI36
NG_031884.1:g.72161del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3033del MANE Select ENSP00000382423.3:p.Cys1012AlafsTer?
ENST00000399503.3:c.3033del ENSP00000382423.3:p.Cys1012AlafsTer?
NM_005921.1:c.3033del NP_005912.1:p.Cys1012AlafsTer?
XM_005248519.3:c.2655del XP_005248576.2:p.Cys886AlafsTer?
XM_011543406.1:c.2778del XP_011541708.1:p.Cys927AlafsTer?
XM_011543407.1:c.2754del XP_011541709.1:p.Cys919AlafsTer?
XM_011543408.1:c.3033del XP_011541710.1:p.Cys1012AlafsTer?
XM_017009484.1:c.2622del XP_016864973.1:p.Cys875AlafsTer?
XM_017009485.1:c.2544del XP_016864974.1:p.Cys849AlafsTer?
XR_001742068.2:n.3064del
NM_005921.2:c.3033del MANE Select NP_005912.1:p.Cys1012AlafsTer?