Canonical Allele Identifier: CA381523000

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353969G>C (hg19) ; chr11:g.67586498G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586498G>C , CM000673.2:g.67586498G>C	GRCh38
NC_000011.9:g.67353969G>C , CM000673.1:g.67353969G>C	GRCh37
NC_000011.8:g.67110545G>C	NCBI36
NG_012075.1:g.7904G>C , LRG_723:g.7904G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.446G>C	ENSP00000381604.1:p.Ser149Thr
ENST00000398606.10:c.554G>C MANE Select	ENSP00000381607.3:p.Ser185Thr
ENST00000646888.1:c.*270G>C	ENSP00000494477.1:n.*270G>C
ENST00000398603.5:c.446G>C	ENSP00000381604.1:p.Ser149Thr
ENST00000398606.7:c.554G>C	ENSP00000381607.3:p.Ser185Thr
ENST00000467591.1:n.665G>C
ENST00000494593.1:n.1526G>C
ENST00000498765.5:c.617G>C
NM_000852.3:c.554G>C , LRG_723t1:c.554G>C	NP_000843.1:p.Ser185Thr
NM_000852.4:c.554G>C MANE Select	NP_000843.1:p.Ser185Thr