Canonical Allele Identifier: CA381521438

Gene: GSTP1

Linked Data

• gnomAD v4: 11-67586196-C-G
• MyVariant Identifiers: chr11:g.67353667C>G (hg19) ; chr11:g.67586196C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586196C>G , CM000673.2:g.67586196C>G	GRCh38
NC_000011.9:g.67353667C>G , CM000673.1:g.67353667C>G	GRCh37
NC_000011.8:g.67110243C>G	NCBI36
NG_012075.1:g.7602C>G , LRG_723:g.7602C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-193C>G	ENSP00000381604.1:n.337-193C>G
ENST00000398606.10:c.429C>G MANE Select	ENSP00000381607.3:p.Phe143Leu
ENST00000646888.1:c.*145C>G	ENSP00000494477.1:n.*145C>G
ENST00000398603.5:c.337-193C>G	ENSP00000381604.1:n.337-193C>G
ENST00000398606.7:c.429C>G	ENSP00000381607.3:p.Phe143Leu
ENST00000467591.1:n.540C>G
ENST00000494593.1:n.1224C>G
ENST00000495996.1:c.93C>G	ENSP00000484686.1:p.Phe31Leu
ENST00000498765.5:c.492C>G
NM_000852.3:c.429C>G , LRG_723t1:c.429C>G	NP_000843.1:p.Phe143Leu
NM_000852.4:c.429C>G MANE Select	NP_000843.1:p.Phe143Leu