Canonical Allele Identifier: CA381522522

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353896C>A (hg19) ; chr11:g.67586425C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586425C>A , CM000673.2:g.67586425C>A	GRCh38
NC_000011.9:g.67353896C>A , CM000673.1:g.67353896C>A	GRCh37
NC_000011.8:g.67110472C>A	NCBI36
NG_012075.1:g.7831C>A , LRG_723:g.7831C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.373C>A	ENSP00000381604.1:p.Leu125Met
ENST00000398606.10:c.481C>A MANE Select	ENSP00000381607.3:p.Leu161Met
ENST00000646888.1:c.*197C>A	ENSP00000494477.1:n.*197C>A
ENST00000398603.5:c.373C>A	ENSP00000381604.1:p.Leu125Met
ENST00000398606.7:c.481C>A	ENSP00000381607.3:p.Leu161Met
ENST00000467591.1:n.592C>A
ENST00000494593.1:n.1453C>A
ENST00000495996.1:c.207C>A	ENSP00000484686.1:p.Cys69Ter
ENST00000498765.5:c.544C>A
NM_000852.3:c.481C>A , LRG_723t1:c.481C>A	NP_000843.1:p.Leu161Met
NM_000852.4:c.481C>A MANE Select	NP_000843.1:p.Leu161Met