Canonical Allele Identifier: CA381522569

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353900T>A (hg19) ; chr11:g.67586429T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586429T>A , CM000673.2:g.67586429T>A	GRCh38
NC_000011.9:g.67353900T>A , CM000673.1:g.67353900T>A	GRCh37
NC_000011.8:g.67110476T>A	NCBI36
NG_012075.1:g.7835T>A , LRG_723:g.7835T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.377T>A	ENSP00000381604.1:p.Ile126Asn
ENST00000398606.10:c.485T>A MANE Select	ENSP00000381607.3:p.Ile162Asn
ENST00000646888.1:c.*201T>A	ENSP00000494477.1:n.*201T>A
ENST00000398603.5:c.377T>A	ENSP00000381604.1:p.Ile126Asn
ENST00000398606.7:c.485T>A	ENSP00000381607.3:p.Ile162Asn
ENST00000467591.1:n.596T>A
ENST00000494593.1:n.1457T>A
ENST00000495996.1:c.211T>A	ENSP00000484686.1:n.211T>A
ENST00000498765.5:c.548T>A
NM_000852.3:c.485T>A , LRG_723t1:c.485T>A	NP_000843.1:p.Ile162Asn
NM_000852.4:c.485T>A MANE Select	NP_000843.1:p.Ile162Asn