Canonical Allele Identifier: CA2646987451

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736938_109736940del , CM000663.2:g.109736938_109736940del GRCh38
NC_000001.10:g.110279560_110279562del , CM000663.1:g.110279560_110279562del GRCh37
NC_000001.9:g.110081083_110081085del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*131_*133del (GSTM3) MANE Select ENSP00000354357.2:n.*131_*133del
ENST00000256594.7:c.*131_*133del (GSTM3) ENSP00000256594.3:n.*131_*133del
ENST00000361066.6:c.*131_*133del (GSTM3) ENSP00000354357.2:n.*131_*133del
ENST00000429410.2:n.82+24590_82+24592del (GSTM5)
ENST00000486823.5:n.773_775del (GSTM3)
NM_000849.4:c.*131_*133del (GSTM3) NP_000840.2:n.*131_*133del
NR_024537.1:n.1043_1045del (GSTM3)
NM_000849.5:c.*131_*133del (GSTM3) MANE Select NP_000840.2:n.*131_*133del
NR_024537.2:n.1043_1045del (GSTM3)