Canonical Allele Identifier: CA600237057

Gene: GSTP1

Linked Data

• dbSNP Id: rs1231566869
• gnomAD v2: 11-67353851-G-T
• gnomAD v4: 11-67586380-G-T
• MyVariant Identifiers: chr11:g.67353851G>T (hg19) ; chr11:g.67586380G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586380G>T , CM000673.2:g.67586380G>T	GRCh38
NC_000011.9:g.67353851G>T , CM000673.1:g.67353851G>T	GRCh37
NC_000011.8:g.67110427G>T	NCBI36
NG_012075.1:g.7786G>T , LRG_723:g.7786G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-9G>T	ENSP00000381604.1:n.337-9G>T
ENST00000398606.10:c.445-9G>T MANE Select	ENSP00000381607.3:n.445-9G>T
ENST00000646888.1:c.*161-9G>T	ENSP00000494477.1:n.*161-9G>T
ENST00000398603.5:c.337-9G>T	ENSP00000381604.1:n.337-9G>T
ENST00000398606.7:c.445-9G>T	ENSP00000381607.3:n.445-9G>T
ENST00000467591.1:n.556-9G>T
ENST00000494593.1:n.1408G>T
ENST00000495996.1:c.171-9G>T	ENSP00000484686.1:n.171-9G>T
ENST00000498765.5:c.508-9G>T
NM_000852.3:c.445-9G>T , LRG_723t1:c.445-9G>T	NP_000843.1:n.445-9G>T
NM_000852.4:c.445-9G>T MANE Select	NP_000843.1:n.445-9G>T