Canonical Allele Identifier: CA381521728

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353694G>C (hg19) ; chr11:g.67586223G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586223G>C , CM000673.2:g.67586223G>C	GRCh38
NC_000011.9:g.67353694G>C , CM000673.1:g.67353694G>C	GRCh37
NC_000011.8:g.67110270G>C	NCBI36
NG_012075.1:g.7629G>C , LRG_723:g.7629G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-166G>C	ENSP00000381604.1:n.337-166G>C
ENST00000398606.10:c.444+12G>C MANE Select	ENSP00000381607.3:n.444+12G>C
ENST00000646888.1:c.*160+12G>C	ENSP00000494477.1:n.*160+12G>C
ENST00000398603.5:c.337-166G>C	ENSP00000381604.1:n.337-166G>C
ENST00000398606.7:c.444+12G>C	ENSP00000381607.3:n.444+12G>C
ENST00000467591.1:n.555+12G>C
ENST00000494593.1:n.1251G>C
ENST00000495996.1:c.120G>C	ENSP00000484686.1:p.Trp40Cys
ENST00000498765.5:c.507+12G>C
NM_000852.3:c.444+12G>C , LRG_723t1:c.444+12G>C	NP_000843.1:n.444+12G>C
NM_000852.4:c.444+12G>C MANE Select	NP_000843.1:n.444+12G>C