Canonical Allele Identifier: CA6142828

Gene: GSTP1

Linked Data

• dbSNP Id: rs11553890
• ExAC: 11:67353610 C / T
• gnomAD v2: 11-67353610-C-T
• gnomAD v3: 11-67586139-C-T
• gnomAD v4: 11-67586139-C-T
• MyVariant Identifiers: chr11:g.67353610C>T (hg19) ; chr11:g.67586139C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586139C>T , CM000673.2:g.67586139C>T	GRCh38
NC_000011.9:g.67353610C>T , CM000673.1:g.67353610C>T	GRCh37
NC_000011.8:g.67110186C>T	NCBI36
NG_012075.1:g.7545C>T , LRG_723:g.7545C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-250C>T	ENSP00000381604.1:n.337-250C>T
ENST00000398606.10:c.372C>T MANE Select	ENSP00000381607.3:p.Pro124=
ENST00000646888.1:c.*88C>T	ENSP00000494477.1:n.*88C>T
ENST00000398603.5:c.337-250C>T	ENSP00000381604.1:n.337-250C>T
ENST00000398606.7:c.372C>T	ENSP00000381607.3:p.Pro124=
ENST00000467591.1:n.483C>T
ENST00000494593.1:n.1167C>T
ENST00000495996.1:c.36C>T	ENSP00000484686.1:p.Pro12=
ENST00000498765.5:c.435C>T
NM_000852.3:c.372C>T , LRG_723t1:c.372C>T	NP_000843.1:p.Pro124=
NM_000852.4:c.372C>T MANE Select	NP_000843.1:p.Pro124=