Canonical Allele Identifier: CA381522932

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353956G>C (hg19) ; chr11:g.67586485G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586485G>C , CM000673.2:g.67586485G>C	GRCh38
NC_000011.9:g.67353956G>C , CM000673.1:g.67353956G>C	GRCh37
NC_000011.8:g.67110532G>C	NCBI36
NG_012075.1:g.7891G>C , LRG_723:g.7891G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.433G>C	ENSP00000381604.1:p.Val145Leu
ENST00000398606.10:c.541G>C MANE Select	ENSP00000381607.3:p.Val181Leu
ENST00000646888.1:c.*257G>C	ENSP00000494477.1:n.*257G>C
ENST00000398603.5:c.433G>C	ENSP00000381604.1:p.Val145Leu
ENST00000398606.7:c.541G>C	ENSP00000381607.3:p.Val181Leu
ENST00000467591.1:n.652G>C
ENST00000494593.1:n.1513G>C
ENST00000498765.5:c.604G>C
NM_000852.3:c.541G>C , LRG_723t1:c.541G>C	NP_000843.1:p.Val181Leu
NM_000852.4:c.541G>C MANE Select	NP_000843.1:p.Val181Leu