Canonical Allele Identifier: CA381522729

Gene: GSTP1

Linked Data

• gnomAD v4: 11-67586452-T-A
• MyVariant Identifiers: chr11:g.67353923T>A (hg19) ; chr11:g.67586452T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586452T>A , CM000673.2:g.67586452T>A	GRCh38
NC_000011.9:g.67353923T>A , CM000673.1:g.67353923T>A	GRCh37
NC_000011.8:g.67110499T>A	NCBI36
NG_012075.1:g.7858T>A , LRG_723:g.7858T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.400T>A	ENSP00000381604.1:p.Cys134Ser
ENST00000398606.10:c.508T>A MANE Select	ENSP00000381607.3:p.Cys170Ser
ENST00000646888.1:c.*224T>A	ENSP00000494477.1:n.*224T>A
ENST00000398603.5:c.400T>A	ENSP00000381604.1:p.Cys134Ser
ENST00000398606.7:c.508T>A	ENSP00000381607.3:p.Cys170Ser
ENST00000467591.1:n.619T>A
ENST00000494593.1:n.1480T>A
ENST00000498765.5:c.571T>A
NM_000852.3:c.508T>A , LRG_723t1:c.508T>A	NP_000843.1:p.Cys170Ser
NM_000852.4:c.508T>A MANE Select	NP_000843.1:p.Cys170Ser