Canonical Allele Identifier: CA381522939

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353957T>C (hg19) ; chr11:g.67586486T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586486T>C , CM000673.2:g.67586486T>C	GRCh38
NC_000011.9:g.67353957T>C , CM000673.1:g.67353957T>C	GRCh37
NC_000011.8:g.67110533T>C	NCBI36
NG_012075.1:g.7892T>C , LRG_723:g.7892T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.434T>C	ENSP00000381604.1:p.Val145Ala
ENST00000398606.10:c.542T>C MANE Select	ENSP00000381607.3:p.Val181Ala
ENST00000646888.1:c.*258T>C	ENSP00000494477.1:n.*258T>C
ENST00000398603.5:c.434T>C	ENSP00000381604.1:p.Val145Ala
ENST00000398606.7:c.542T>C	ENSP00000381607.3:p.Val181Ala
ENST00000467591.1:n.653T>C
ENST00000494593.1:n.1514T>C
ENST00000498765.5:c.605T>C
NM_000852.3:c.542T>C , LRG_723t1:c.542T>C	NP_000843.1:p.Val181Ala
NM_000852.4:c.542T>C MANE Select	NP_000843.1:p.Val181Ala