Canonical Allele Identifier: CA381522783

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353930A>C (hg19) ; chr11:g.67586459A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586459A>C , CM000673.2:g.67586459A>C	GRCh38
NC_000011.9:g.67353930A>C , CM000673.1:g.67353930A>C	GRCh37
NC_000011.8:g.67110506A>C	NCBI36
NG_012075.1:g.7865A>C , LRG_723:g.7865A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.407A>C	ENSP00000381604.1:p.Asp136Ala
ENST00000398606.10:c.515A>C MANE Select	ENSP00000381607.3:p.Asp172Ala
ENST00000646888.1:c.*231A>C	ENSP00000494477.1:n.*231A>C
ENST00000398603.5:c.407A>C	ENSP00000381604.1:p.Asp136Ala
ENST00000398606.7:c.515A>C	ENSP00000381607.3:p.Asp172Ala
ENST00000467591.1:n.626A>C
ENST00000494593.1:n.1487A>C
ENST00000498765.5:c.578A>C
NM_000852.3:c.515A>C , LRG_723t1:c.515A>C	NP_000843.1:p.Asp172Ala
NM_000852.4:c.515A>C MANE Select	NP_000843.1:p.Asp172Ala