Canonical Allele Identifier: CA381522322

Gene: GSTP1

Linked Data

• dbSNP Id: rs1591100754
• MyVariant Identifiers: chr11:g.67353871T>C (hg19) ; chr11:g.67586400T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586400T>C , CM000673.2:g.67586400T>C	GRCh38
NC_000011.9:g.67353871T>C , CM000673.1:g.67353871T>C	GRCh37
NC_000011.8:g.67110447T>C	NCBI36
NG_012075.1:g.7806T>C , LRG_723:g.7806T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.348T>C	ENSP00000381604.1:p.Ala116=
ENST00000398606.10:c.456T>C MANE Select	ENSP00000381607.3:p.Ala152=
ENST00000646888.1:c.*172T>C	ENSP00000494477.1:n.*172T>C
ENST00000398603.5:c.348T>C	ENSP00000381604.1:p.Ala116=
ENST00000398606.7:c.456T>C	ENSP00000381607.3:p.Ala152=
ENST00000467591.1:n.567T>C
ENST00000494593.1:n.1428T>C
ENST00000495996.1:c.182T>C	ENSP00000484686.1:p.Leu61Pro
ENST00000498765.5:c.519T>C
NM_000852.3:c.456T>C , LRG_723t1:c.456T>C	NP_000843.1:p.Ala152=
NM_000852.4:c.456T>C MANE Select	NP_000843.1:p.Ala152=