Canonical Allele Identifier: CA2646985002

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109734274del , CM000663.2:g.109734274del GRCh38
NC_000001.10:g.110276896del , CM000663.1:g.110276896del GRCh37
NC_000001.9:g.110078419del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*2799del (GSTM3) MANE Select ENSP00000354357.2:n.*2799del
ENST00000256594.7:c.*2799del (GSTM3) ENSP00000256594.3:n.*2799del
ENST00000429410.2:n.82+21926del (GSTM5)
NM_000849.4:c.*2799del (GSTM3) NP_000840.2:n.*2799del
NR_024537.1:n.3711del (GSTM3)
NM_000849.5:c.*2799del (GSTM3) MANE Select NP_000840.2:n.*2799del
NR_024537.2:n.3711del (GSTM3)