Canonical Allele Identifier: CA2832543258
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875195dup , CM000667.2:g.56875195dup GRCh38
NC_000005.9:g.56171022dup , CM000667.1:g.56171022dup GRCh37
NC_000005.8:g.56206779dup NCBI36
NG_031884.1:g.65123dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.1850dup MANE Select ENSP00000382423.3:p.Ala618SerfsTer28
ENST00000399503.3:c.1850dup ENSP00000382423.3:p.Ala618SerfsTer28
NM_005921.1:c.1850dup NP_005912.1:p.Ala618SerfsTer28
XM_005248519.3:c.1472dup XP_005248576.2:p.Ala492SerfsTer28
XM_011543406.1:c.1595dup XP_011541708.1:p.Ala533SerfsTer28
XM_011543407.1:c.1686+2190dup XP_011541709.1:n.1686+2190dup
XM_011543408.1:c.1850dup XP_011541710.1:p.Ala618SerfsTer28
XM_017009484.1:c.1439dup XP_016864973.1:p.Ala481SerfsTer28
XM_017009485.1:c.1361dup XP_016864974.1:p.Ala455SerfsTer28
XR_001742068.2:n.1881dup
NM_005921.2:c.1850dup MANE Select NP_005912.1:p.Ala618SerfsTer28