Canonical Allele Identifier: CA224154661

Gene: GSTP1

Linked Data

• dbSNP Id: rs975116633
• gnomAD v2: 11-67353284-A-C
• gnomAD v3: 11-67585813-A-C
• gnomAD v4: 11-67585813-A-C
• MyVariant Identifiers: chr11:g.67353284A>C (hg19) ; chr11:g.67585813A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585813A>C , CM000673.2:g.67585813A>C	GRCh38
NC_000011.9:g.67353284A>C , CM000673.1:g.67353284A>C	GRCh37
NC_000011.8:g.67109860A>C	NCBI36
NG_012075.1:g.7219A>C , LRG_723:g.7219A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000398603.6:c.336+572A>C	ENSP00000381604.1:n.336+572A>C
ENST00000398606.10:c.337-291A>C MANE Select	ENSP00000381607.3:n.337-291A>C
ENST00000646888.1:c.*53-291A>C	ENSP00000494477.1:n.*53-291A>C
ENST00000398603.5:c.336+572A>C	ENSP00000381604.1:n.336+572A>C
ENST00000398606.7:c.337-291A>C	ENSP00000381607.3:n.337-291A>C
ENST00000467591.1:n.448-291A>C
ENST00000494593.1:n.1132-291A>C
ENST00000498765.5:c.400-291A>C
NM_000852.3:c.337-291A>C , LRG_723t1:c.337-291A>C	NP_000843.1:n.337-291A>C
NM_000852.4:c.337-291A>C MANE Select	NP_000843.1:n.337-291A>C