Canonical Allele Identifier: CA2695204651
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882311del , CM000667.2:g.56882311del GRCh38
NC_000005.9:g.56178138del , CM000667.1:g.56178138del GRCh37
NC_000005.8:g.56213895del NCBI36
NG_031884.1:g.72239del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3111del MANE Select ENSP00000382423.3:p.Asp1038ThrfsTer?
ENST00000399503.3:c.3111del ENSP00000382423.3:p.Asp1038ThrfsTer?
NM_005921.1:c.3111del NP_005912.1:p.Asp1038ThrfsTer?
XM_005248519.3:c.2733del XP_005248576.2:p.Asp912ThrfsTer?
XM_011543406.1:c.2856del XP_011541708.1:p.Asp953ThrfsTer?
XM_011543407.1:c.2832del XP_011541709.1:p.Asp945ThrfsTer?
XM_011543408.1:c.3111del XP_011541710.1:p.Asp1038ThrfsTer?
XM_017009484.1:c.2700del XP_016864973.1:p.Asp901ThrfsTer?
XM_017009485.1:c.2622del XP_016864974.1:p.Asp875ThrfsTer?
XR_001742068.2:n.3142del
NM_005921.2:c.3111del MANE Select NP_005912.1:p.Asp1038ThrfsTer?