Canonical Allele Identifier: CA381522945

Gene: GSTP1

Linked Data

• gnomAD v4: 11-67586488-G-T
• MyVariant Identifiers: chr11:g.67353959G>T (hg19) ; chr11:g.67586488G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586488G>T , CM000673.2:g.67586488G>T	GRCh38
NC_000011.9:g.67353959G>T , CM000673.1:g.67353959G>T	GRCh37
NC_000011.8:g.67110535G>T	NCBI36
NG_012075.1:g.7894G>T , LRG_723:g.7894G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.436G>T	ENSP00000381604.1:p.Gly146Trp
ENST00000398606.10:c.544G>T MANE Select	ENSP00000381607.3:p.Gly182Trp
ENST00000646888.1:c.*260G>T	ENSP00000494477.1:n.*260G>T
ENST00000398603.5:c.436G>T	ENSP00000381604.1:p.Gly146Trp
ENST00000398606.7:c.544G>T	ENSP00000381607.3:p.Gly182Trp
ENST00000467591.1:n.655G>T
ENST00000494593.1:n.1516G>T
ENST00000498765.5:c.607G>T
NM_000852.3:c.544G>T , LRG_723t1:c.544G>T	NP_000843.1:p.Gly182Trp
NM_000852.4:c.544G>T MANE Select	NP_000843.1:p.Gly182Trp