Canonical Allele Identifier: CA1188220375

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736819_109736820delinsTC , CM000663.2:g.109736819_109736820delinsTC GRCh38
NC_000001.10:g.110279441_110279442delinsTC , CM000663.1:g.110279441_110279442delinsTC GRCh37
NC_000001.9:g.110080964_110080965delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*251_*252delinsGA (GSTM3) MANE Select ENSP00000354357.2:n.*251_*252delinsGA
ENST00000256594.7:c.*251_*252delinsGA (GSTM3) ENSP00000256594.3:n.*251_*252delinsGA
ENST00000361066.6:c.*251_*252delinsGA (GSTM3) ENSP00000354357.2:n.*251_*252delinsGA
ENST00000429410.2:n.82+24471_82+24472delinsTC (GSTM5)
NM_000849.4:c.*251_*252delinsGA (GSTM3) NP_000840.2:n.*251_*252delinsGA
NR_024537.1:n.1163_1164delinsGA (GSTM3)
NM_000849.5:c.*251_*252delinsGA (GSTM3) MANE Select NP_000840.2:n.*251_*252delinsGA
NR_024537.2:n.1163_1164delinsGA (GSTM3)