Canonical Allele Identifier: CA381515586

Gene: GSTP1

Linked Data

• dbSNP Id: rs1217728595
• gnomAD v2: 11-67352172-C-G
• gnomAD v4: 11-67584701-C-G
• MyVariant Identifiers: chr11:g.67352172C>G (hg19) ; chr11:g.67584701C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67584701C>G , CM000673.2:g.67584701C>G	GRCh38
NC_000011.9:g.67352172C>G , CM000673.1:g.67352172C>G	GRCh37
NC_000011.8:g.67108748C>G	NCBI36
NG_012075.1:g.6107C>G , LRG_723:g.6107C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.161C>G	ENSP00000381604.1:p.Pro54Arg
ENST00000398606.10:c.161C>G MANE Select	ENSP00000381607.3:p.Pro54Arg
ENST00000646888.1:c.54C>G	ENSP00000494477.1:p.Pro18=
ENST00000398603.5:c.161C>G	ENSP00000381604.1:p.Pro54Arg
ENST00000398606.7:c.161C>G	ENSP00000381607.3:p.Pro54Arg
ENST00000489040.1:n.160C>G
ENST00000494593.1:n.591C>G
ENST00000498765.5:c.124C>G
NM_000852.3:c.161C>G , LRG_723t1:c.161C>G	NP_000843.1:p.Pro54Arg
NM_000852.4:c.161C>G MANE Select	NP_000843.1:p.Pro54Arg