Canonical Allele Identifier: CA2696682671

Linked Data

dbSNP Id: rs2101349105

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737176_109737177insCCTTCAGGTTTGG , CM000663.2:g.109737176_109737177insCCTTCAGGTTTGG GRCh38
NC_000001.10:g.110279798_110279799insCCTTCAGGTTTGG , CM000663.1:g.110279798_110279799insCCTTCAGGTTTGG GRCh37
NC_000001.9:g.110081321_110081322insCCTTCAGGTTTGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.580-7_580-6insCAAACCTGAAGGC (GSTM3) MANE Select ENSP00000354357.2:n.580-7_580-6insCAAACCTGAAGGC
ENST00000256594.7:c.580-7_580-6insCAAACCTGAAGGC (GSTM3) ENSP00000256594.3:n.580-7_580-6insCAAACCTGAAGGC
ENST00000361066.6:c.580-7_580-6insCAAACCTGAAGGC (GSTM3) ENSP00000354357.2:n.580-7_580-6insCAAACCTGAAGGC
ENST00000429410.2:n.82+24828_82+24829insCCTTCAGGTTTGG (GSTM5)
ENST00000476321.5:n.541_542insCAAACCTGAAGGC (GSTM3)
ENST00000486823.5:n.544-7_544-6insCAAACCTGAAGGC (GSTM3)
ENST00000488824.1:n.925-7_925-6insCAAACCTGAAGGC (GSTM3)
NM_000849.4:c.580-7_580-6insCAAACCTGAAGGC (GSTM3) NP_000840.2:n.580-7_580-6insCAAACCTGAAGGC
NR_024537.1:n.814-7_814-6insCAAACCTGAAGGC (GSTM3)
XM_011541296.1:c.799-7_799-6insCAAACCTGAAGGC (GSTM3) XP_011539598.1:n.799-7_799-6insCAAACCTGAAGGC
NM_000849.5:c.580-7_580-6insCAAACCTGAAGGC (GSTM3) MANE Select NP_000840.2:n.580-7_580-6insCAAACCTGAAGGC
NR_024537.2:n.814-7_814-6insCAAACCTGAAGGC (GSTM3)