Canonical Allele Identifier: CA6142846

Gene: GSTP1

Linked Data

• dbSNP Id: rs772064183
• ExAC: 11:67353679 C / T
• gnomAD v2: 11-67353679-C-T
• gnomAD v3: 11-67586208-C-T
• gnomAD v4: 11-67586208-C-T
• MyVariant Identifiers: chr11:g.67353679C>T (hg19) ; chr11:g.67586208C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586208C>T , CM000673.2:g.67586208C>T	GRCh38
NC_000011.9:g.67353679C>T , CM000673.1:g.67353679C>T	GRCh37
NC_000011.8:g.67110255C>T	NCBI36
NG_012075.1:g.7614C>T , LRG_723:g.7614C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-181C>T	ENSP00000381604.1:n.337-181C>T
ENST00000398606.10:c.441C>T MANE Select	ENSP00000381607.3:p.Asp147=
ENST00000646888.1:c.*157C>T	ENSP00000494477.1:n.*157C>T
ENST00000398603.5:c.337-181C>T	ENSP00000381604.1:n.337-181C>T
ENST00000398606.7:c.441C>T	ENSP00000381607.3:p.Asp147=
ENST00000467591.1:n.552C>T
ENST00000494593.1:n.1236C>T
ENST00000495996.1:c.105C>T	ENSP00000484686.1:p.Asp35=
ENST00000498765.5:c.504C>T
NM_000852.3:c.441C>T , LRG_723t1:c.441C>T	NP_000843.1:p.Asp147=
NM_000852.4:c.441C>T MANE Select	NP_000843.1:p.Asp147=