Canonical Allele Identifier: CA2646987118

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736728_109736729del , CM000663.2:g.109736728_109736729del GRCh38
NC_000001.10:g.110279350_110279351del , CM000663.1:g.110279350_110279351del GRCh37
NC_000001.9:g.110080873_110080874del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*345_*346del (GSTM3) MANE Select ENSP00000354357.2:n.*345_*346del
ENST00000256594.7:c.*345_*346del (GSTM3) ENSP00000256594.3:n.*345_*346del
ENST00000361066.6:c.*345_*346del (GSTM3) ENSP00000354357.2:n.*345_*346del
ENST00000429410.2:n.82+24380_82+24381del (GSTM5)
NM_000849.4:c.*345_*346del (GSTM3) NP_000840.2:n.*345_*346del
NR_024537.1:n.1257_1258del (GSTM3)
NM_000849.5:c.*345_*346del (GSTM3) MANE Select NP_000840.2:n.*345_*346del
NR_024537.2:n.1257_1258del (GSTM3)