Canonical Allele Identifier: CA381521041

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353632A>C (hg19) ; chr11:g.67586161A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586161A>C , CM000673.2:g.67586161A>C	GRCh38
NC_000011.9:g.67353632A>C , CM000673.1:g.67353632A>C	GRCh37
NC_000011.8:g.67110208A>C	NCBI36
NG_012075.1:g.7567A>C , LRG_723:g.7567A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-228A>C	ENSP00000381604.1:n.337-228A>C
ENST00000398606.10:c.394A>C MANE Select	ENSP00000381607.3:p.Thr132Pro
ENST00000646888.1:c.*110A>C	ENSP00000494477.1:n.*110A>C
ENST00000398603.5:c.337-228A>C	ENSP00000381604.1:n.337-228A>C
ENST00000398606.7:c.394A>C	ENSP00000381607.3:p.Thr132Pro
ENST00000467591.1:n.505A>C
ENST00000494593.1:n.1189A>C
ENST00000495996.1:c.58A>C	ENSP00000484686.1:p.Thr20Pro
ENST00000498765.5:c.457A>C
NM_000852.3:c.394A>C , LRG_723t1:c.394A>C	NP_000843.1:p.Thr132Pro
NM_000852.4:c.394A>C MANE Select	NP_000843.1:p.Thr132Pro