Canonical Allele Identifier: CA2646987235

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736784_109736785del , CM000663.2:g.109736784_109736785del GRCh38
NC_000001.10:g.110279406_110279407del , CM000663.1:g.110279406_110279407del GRCh37
NC_000001.9:g.110080929_110080930del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*291_*292del (GSTM3) MANE Select ENSP00000354357.2:n.*291_*292del
ENST00000256594.7:c.*291_*292del (GSTM3) ENSP00000256594.3:n.*291_*292del
ENST00000361066.6:c.*291_*292del (GSTM3) ENSP00000354357.2:n.*291_*292del
ENST00000429410.2:n.82+24436_82+24437del (GSTM5)
NM_000849.4:c.*291_*292del (GSTM3) NP_000840.2:n.*291_*292del
NR_024537.1:n.1203_1204del (GSTM3)
NM_000849.5:c.*291_*292del (GSTM3) MANE Select NP_000840.2:n.*291_*292del
NR_024537.2:n.1203_1204del (GSTM3)