Canonical Allele Identifier: CA1980212229
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67583921C= , CM000673.2:g.67583921C= GRCh38
NC_000011.9:g.67351392C= , CM000673.1:g.67351392C= GRCh37
NC_000011.8:g.67107968C= NCBI36
NG_012075.1:g.5327C= , LRG_723:g.5327C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.1+77C= ENSP00000381604.1:n.1+77C=
ENST00000398606.10:c.1+77C= MANE Select ENSP00000381607.3:n.1+77C=
ENST00000646888.1:c.1+77C= ENSP00000494477.1:n.1+77C=
ENST00000398603.5:c.1+77C= ENSP00000381604.1:n.1+77C=
ENST00000398606.7:c.1+77C= ENSP00000381607.3:n.1+77C=
ENST00000494593.1:n.23+77C=
NM_000852.3:c.1+77C= , LRG_723t1:c.1+77C= NP_000843.1:n.1+77C=
NM_000852.4:c.1+77C= MANE Select NP_000843.1:n.1+77C=