Canonical Allele Identifier: CA2646987096

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736715_109736716del , CM000663.2:g.109736715_109736716del GRCh38
NC_000001.10:g.110279337_110279338del , CM000663.1:g.110279337_110279338del GRCh37
NC_000001.9:g.110080860_110080861del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*357_*358del (GSTM3) MANE Select ENSP00000354357.2:n.*357_*358del
ENST00000256594.7:c.*357_*358del (GSTM3) ENSP00000256594.3:n.*357_*358del
ENST00000361066.6:c.*357_*358del (GSTM3) ENSP00000354357.2:n.*357_*358del
ENST00000429410.2:n.82+24367_82+24368del (GSTM5)
NM_000849.4:c.*357_*358del (GSTM3) NP_000840.2:n.*357_*358del
NR_024537.1:n.1269_1270del (GSTM3)
NM_000849.5:c.*357_*358del (GSTM3) MANE Select NP_000840.2:n.*357_*358del
NR_024537.2:n.1269_1270del (GSTM3)