Canonical Allele Identifier: CA2696682575

Linked Data

dbSNP Id: rs2101349086

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737171_109737172insCAAAACGGCACAT , CM000663.2:g.109737171_109737172insCAAAACGGCACAT GRCh38
NC_000001.10:g.110279793_110279794insCAAAACGGCACAT , CM000663.1:g.110279793_110279794insCAAAACGGCACAT GRCh37
NC_000001.9:g.110081316_110081317insCAAAACGGCACAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.580-2_580-1insTGTGCCGTTTTGA (GSTM3) MANE Select ENSP00000354357.2:n.580-2_580-1insTGTGCCGTTTTGA
ENST00000256594.7:c.580-2_580-1insTGTGCCGTTTTGA (GSTM3) ENSP00000256594.3:n.580-2_580-1insTGTGCCGTTTTGA
ENST00000361066.6:c.580-2_580-1insTGTGCCGTTTTGA (GSTM3) ENSP00000354357.2:n.580-2_580-1insTGTGCCGTTTTGA
ENST00000429410.2:n.82+24823_82+24824insCAAAACGGCACAT (GSTM5)
ENST00000476321.5:n.546_547insTGTGCCGTTTTGA (GSTM3)
ENST00000486823.5:n.544-2_544-1insTGTGCCGTTTTGA (GSTM3)
ENST00000488824.1:n.925-2_925-1insTGTGCCGTTTTGA (GSTM3)
NM_000849.4:c.580-2_580-1insTGTGCCGTTTTGA (GSTM3) NP_000840.2:n.580-2_580-1insTGTGCCGTTTTGA
NR_024537.1:n.814-2_814-1insTGTGCCGTTTTGA (GSTM3)
XM_011541296.1:c.799-2_799-1insTGTGCCGTTTTGA (GSTM3) XP_011539598.1:n.799-2_799-1insTGTGCCGTTTTGA
NM_000849.5:c.580-2_580-1insTGTGCCGTTTTGA (GSTM3) MANE Select NP_000840.2:n.580-2_580-1insTGTGCCGTTTTGA
NR_024537.2:n.814-2_814-1insTGTGCCGTTTTGA (GSTM3)