Canonical Allele Identifier: CA1980214901
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585279_67585280delinsAC , CM000673.2:g.67585279_67585280delinsAC GRCh38
NC_000011.9:g.67352750_67352751delinsAC , CM000673.1:g.67352750_67352751delinsAC GRCh37
NC_000011.8:g.67109326_67109327delinsAC NCBI36
NG_012075.1:g.6685_6686delinsAC , LRG_723:g.6685_6686delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.336+38_336+39delinsAC ENSP00000381604.1:n.336+38_336+39delinsAC
ENST00000398606.10:c.336+38_336+39delinsAC MANE Select ENSP00000381607.3:n.336+38_336+39delinsAC
ENST00000646888.1:c.*52+38_*52+39delinsAC ENSP00000494477.1:n.*52+38_*52+39delinsAC
ENST00000398603.5:c.336+38_336+39delinsAC ENSP00000381604.1:n.336+38_336+39delinsAC
ENST00000398606.7:c.336+38_336+39delinsAC ENSP00000381607.3:n.336+38_336+39delinsAC
ENST00000467591.1:n.447+38_447+39delinsAC
ENST00000494593.1:n.1131+38_1131+39delinsAC
ENST00000498765.5:c.399+38_399+39delinsAC
NM_000852.3:c.336+38_336+39delinsAC , LRG_723t1:c.336+38_336+39delinsAC NP_000843.1:n.336+38_336+39delinsAC
NM_000852.4:c.336+38_336+39delinsAC MANE Select NP_000843.1:n.336+38_336+39delinsAC