Canonical Allele Identifier: CA1188220532

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737271_109737272delinsAT , CM000663.2:g.109737271_109737272delinsAT GRCh38
NC_000001.10:g.110279893_110279894delinsAT , CM000663.1:g.110279893_110279894delinsAT GRCh37
NC_000001.9:g.110081416_110081417delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.580-103_580-102delinsAT (GSTM3) MANE Select ENSP00000354357.2:n.580-103_580-102delinsAT
ENST00000256594.7:c.580-103_580-102delinsAT (GSTM3) ENSP00000256594.3:n.580-103_580-102delinsAT
ENST00000361066.6:c.580-103_580-102delinsAT (GSTM3) ENSP00000354357.2:n.580-103_580-102delinsAT
ENST00000429410.2:n.82+24923_82+24924delinsAT (GSTM5)
ENST00000476321.5:n.445_446delinsAT (GSTM3)
ENST00000486823.5:n.544-103_544-102delinsAT (GSTM3)
ENST00000488824.1:n.925-103_925-102delinsAT (GSTM3)
NM_000849.4:c.580-103_580-102delinsAT (GSTM3) NP_000840.2:n.580-103_580-102delinsAT
NR_024537.1:n.814-103_814-102delinsAT (GSTM3)
XM_011541296.1:c.799-103_799-102delinsAT (GSTM3) XP_011539598.1:n.799-103_799-102delinsAT
NM_000849.5:c.580-103_580-102delinsAT (GSTM3) MANE Select NP_000840.2:n.580-103_580-102delinsAT
NR_024537.2:n.814-103_814-102delinsAT (GSTM3)