Canonical Allele Identifier: CA381521652

Gene: GSTP1

Linked Data

• gnomAD v4: 11-67586218-A-C
• MyVariant Identifiers: chr11:g.67353689A>C (hg19) ; chr11:g.67586218A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586218A>C , CM000673.2:g.67586218A>C	GRCh38
NC_000011.9:g.67353689A>C , CM000673.1:g.67353689A>C	GRCh37
NC_000011.8:g.67110265A>C	NCBI36
NG_012075.1:g.7624A>C , LRG_723:g.7624A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-171A>C	ENSP00000381604.1:n.337-171A>C
ENST00000398606.10:c.444+7A>C MANE Select	ENSP00000381607.3:n.444+7A>C
ENST00000646888.1:c.*160+7A>C	ENSP00000494477.1:n.*160+7A>C
ENST00000398603.5:c.337-171A>C	ENSP00000381604.1:n.337-171A>C
ENST00000398606.7:c.444+7A>C	ENSP00000381607.3:n.444+7A>C
ENST00000467591.1:n.555+7A>C
ENST00000494593.1:n.1246A>C
ENST00000495996.1:c.115A>C	ENSP00000484686.1:p.Ile39Leu
ENST00000498765.5:c.507+7A>C
NM_000852.3:c.444+7A>C , LRG_723t1:c.444+7A>C	NP_000843.1:n.444+7A>C
NM_000852.4:c.444+7A>C MANE Select	NP_000843.1:n.444+7A>C