Canonical Allele Identifier: CA679523431

Gene: GSTP1

Linked Data

• dbSNP Id: rs1238514438
• gnomAD v3: 11-67586336-A-G
• gnomAD v4: 11-67586336-A-G
• MyVariant Identifiers: chr11:g.67353807A>G (hg19) ; chr11:g.67586336A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586336A>G , CM000673.2:g.67586336A>G	GRCh38
NC_000011.9:g.67353807A>G , CM000673.1:g.67353807A>G	GRCh37
NC_000011.8:g.67110383A>G	NCBI36
NG_012075.1:g.7742A>G , LRG_723:g.7742A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-53A>G	ENSP00000381604.1:n.337-53A>G
ENST00000398606.10:c.445-53A>G MANE Select	ENSP00000381607.3:n.445-53A>G
ENST00000646888.1:c.*161-53A>G	ENSP00000494477.1:n.*161-53A>G
ENST00000398603.5:c.337-53A>G	ENSP00000381604.1:n.337-53A>G
ENST00000398606.7:c.445-53A>G	ENSP00000381607.3:n.445-53A>G
ENST00000467591.1:n.556-53A>G
ENST00000494593.1:n.1364A>G
ENST00000495996.1:c.171-53A>G	ENSP00000484686.1:n.171-53A>G
ENST00000498765.5:c.508-53A>G
NM_000852.3:c.445-53A>G , LRG_723t1:c.445-53A>G	NP_000843.1:n.445-53A>G
NM_000852.4:c.445-53A>G MANE Select	NP_000843.1:n.445-53A>G