Canonical Allele Identifier: CA381521771

Gene: GSTP1

Linked Data

• gnomAD v4: 11-67586225-C-A
• MyVariant Identifiers: chr11:g.67353696C>A (hg19) ; chr11:g.67586225C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586225C>A , CM000673.2:g.67586225C>A	GRCh38
NC_000011.9:g.67353696C>A , CM000673.1:g.67353696C>A	GRCh37
NC_000011.8:g.67110272C>A	NCBI36
NG_012075.1:g.7631C>A , LRG_723:g.7631C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-164C>A	ENSP00000381604.1:n.337-164C>A
ENST00000398606.10:c.444+14C>A MANE Select	ENSP00000381607.3:n.444+14C>A
ENST00000646888.1:c.*160+14C>A	ENSP00000494477.1:n.*160+14C>A
ENST00000398603.5:c.337-164C>A	ENSP00000381604.1:n.337-164C>A
ENST00000398606.7:c.444+14C>A	ENSP00000381607.3:n.444+14C>A
ENST00000467591.1:n.555+14C>A
ENST00000494593.1:n.1253C>A
ENST00000495996.1:c.122C>A	ENSP00000484686.1:p.Pro41His
ENST00000498765.5:c.507+14C>A
NM_000852.3:c.444+14C>A , LRG_723t1:c.444+14C>A	NP_000843.1:n.444+14C>A
NM_000852.4:c.444+14C>A MANE Select	NP_000843.1:n.444+14C>A