Canonical Allele Identifier: CA2646987866

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737242_109737245del , CM000663.2:g.109737242_109737245del GRCh38
NC_000001.10:g.110279864_110279867del , CM000663.1:g.110279864_110279867del GRCh37
NC_000001.9:g.110081387_110081390del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.580-74_580-71del (GSTM3) MANE Select ENSP00000354357.2:n.580-74_580-71del
ENST00000256594.7:c.580-74_580-71del (GSTM3) ENSP00000256594.3:n.580-74_580-71del
ENST00000361066.6:c.580-74_580-71del (GSTM3) ENSP00000354357.2:n.580-74_580-71del
ENST00000429410.2:n.82+24894_82+24897del (GSTM5)
ENST00000476321.5:n.474_477del (GSTM3)
ENST00000486823.5:n.544-74_544-71del (GSTM3)
ENST00000488824.1:n.925-74_925-71del (GSTM3)
NM_000849.4:c.580-74_580-71del (GSTM3) NP_000840.2:n.580-74_580-71del
NR_024537.1:n.814-74_814-71del (GSTM3)
XM_011541296.1:c.799-74_799-71del (GSTM3) XP_011539598.1:n.799-74_799-71del
NM_000849.5:c.580-74_580-71del (GSTM3) MANE Select NP_000840.2:n.580-74_580-71del
NR_024537.2:n.814-74_814-71del (GSTM3)