Canonical Allele Identifier: CA2708987935
Gene: MAP3K1 HGNC NCBI

Linked Data

dbSNP Id: rs2111945894

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882331del , CM000667.2:g.56882331del GRCh38
NC_000005.9:g.56178158del , CM000667.1:g.56178158del GRCh37
NC_000005.8:g.56213915del NCBI36
NG_031884.1:g.72259del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3131del MANE Select ENSP00000382423.3:p.Pro1044GlnfsTer?
ENST00000399503.3:c.3131del ENSP00000382423.3:p.Pro1044GlnfsTer?
NM_005921.1:c.3131del NP_005912.1:p.Pro1044GlnfsTer?
XM_005248519.3:c.2753del XP_005248576.2:p.Pro918GlnfsTer?
XM_011543406.1:c.2876del XP_011541708.1:p.Pro959GlnfsTer?
XM_011543407.1:c.2852del XP_011541709.1:p.Pro951GlnfsTer?
XM_011543408.1:c.3131del XP_011541710.1:p.Pro1044GlnfsTer?
XM_017009484.1:c.2720del XP_016864973.1:p.Pro907GlnfsTer?
XM_017009485.1:c.2642del XP_016864974.1:p.Pro881GlnfsTer?
XR_001742068.2:n.3162del
NM_005921.2:c.3131del MANE Select NP_005912.1:p.Pro1044GlnfsTer?