Canonical Allele Identifier: CA381522005

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353723C>G (hg19) ; chr11:g.67586252C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586252C>G , CM000673.2:g.67586252C>G	GRCh38
NC_000011.9:g.67353723C>G , CM000673.1:g.67353723C>G	GRCh37
NC_000011.8:g.67110299C>G	NCBI36
NG_012075.1:g.7658C>G , LRG_723:g.7658C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-137C>G	ENSP00000381604.1:n.337-137C>G
ENST00000398606.10:c.444+41C>G MANE Select	ENSP00000381607.3:n.444+41C>G
ENST00000646888.1:c.*160+41C>G	ENSP00000494477.1:n.*160+41C>G
ENST00000398603.5:c.337-137C>G	ENSP00000381604.1:n.337-137C>G
ENST00000398606.7:c.444+41C>G	ENSP00000381607.3:n.444+41C>G
ENST00000467591.1:n.555+41C>G
ENST00000494593.1:n.1280C>G
ENST00000495996.1:c.149C>G	ENSP00000484686.1:p.Ser50Cys
ENST00000498765.5:c.507+41C>G
NM_000852.3:c.444+41C>G , LRG_723t1:c.444+41C>G	NP_000843.1:n.444+41C>G
NM_000852.4:c.444+41C>G MANE Select	NP_000843.1:n.444+41C>G