Canonical Allele Identifier: CA475395146
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352242T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584771T>C , CM000673.2:g.67584771T>C GRCh38
NC_000011.9:g.67352242T>C , CM000673.1:g.67352242T>C GRCh37
NC_000011.8:g.67108818T>C NCBI36
NG_012075.1:g.6177T>C , LRG_723:g.6177T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.231T>C ENSP00000381604.1:p.Leu77=
ENST00000398606.10:c.231T>C MANE Select ENSP00000381607.3:p.Leu77=
ENST00000646888.1:c.124T>C ENSP00000494477.1:p.Trp42Arg
ENST00000398603.5:c.231T>C ENSP00000381604.1:p.Leu77=
ENST00000398606.7:c.231T>C ENSP00000381607.3:p.Leu77=
ENST00000489040.1:n.230T>C
ENST00000494593.1:n.661T>C
ENST00000498765.5:c.194T>C
NM_000852.3:c.231T>C , LRG_723t1:c.231T>C NP_000843.1:p.Leu77=
NM_000852.4:c.231T>C MANE Select NP_000843.1:p.Leu77=