Canonical Allele Identifier: CA381522289

Gene: GSTP1

Linked Data

• gnomAD v4: 11-67586397-C-A
• MyVariant Identifiers: chr11:g.67353868C>A (hg19) ; chr11:g.67586397C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586397C>A , CM000673.2:g.67586397C>A	GRCh38
NC_000011.9:g.67353868C>A , CM000673.1:g.67353868C>A	GRCh37
NC_000011.8:g.67110444C>A	NCBI36
NG_012075.1:g.7803C>A , LRG_723:g.7803C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.345C>A	ENSP00000381604.1:p.Phe115Leu
ENST00000398606.10:c.453C>A MANE Select	ENSP00000381607.3:p.Phe151Leu
ENST00000646888.1:c.*169C>A	ENSP00000494477.1:n.*169C>A
ENST00000398603.5:c.345C>A	ENSP00000381604.1:p.Phe115Leu
ENST00000398606.7:c.453C>A	ENSP00000381607.3:p.Phe151Leu
ENST00000467591.1:n.564C>A
ENST00000494593.1:n.1425C>A
ENST00000495996.1:c.179C>A	ENSP00000484686.1:p.Ser60Ter
ENST00000498765.5:c.516C>A
NM_000852.3:c.453C>A , LRG_723t1:c.453C>A	NP_000843.1:p.Phe151Leu
NM_000852.4:c.453C>A MANE Select	NP_000843.1:p.Phe151Leu