Canonical Allele Identifier: CA475395995
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353604A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586133A>C , CM000673.2:g.67586133A>C GRCh38
NC_000011.9:g.67353604A>C , CM000673.1:g.67353604A>C GRCh37
NC_000011.8:g.67110180A>C NCBI36
NG_012075.1:g.7539A>C , LRG_723:g.7539A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-256A>C ENSP00000381604.1:n.337-256A>C
ENST00000398606.10:c.366A>C MANE Select ENSP00000381607.3:p.Ala122=
ENST00000646888.1:c.*82A>C ENSP00000494477.1:n.*82A>C
ENST00000398603.5:c.337-256A>C ENSP00000381604.1:n.337-256A>C
ENST00000398606.7:c.366A>C ENSP00000381607.3:p.Ala122=
ENST00000467591.1:n.477A>C
ENST00000494593.1:n.1161A>C
ENST00000495996.1:c.30A>C ENSP00000484686.1:p.Ala10=
ENST00000498765.5:c.429A>C
NM_000852.3:c.366A>C , LRG_723t1:c.366A>C NP_000843.1:p.Ala122=
NM_000852.4:c.366A>C MANE Select NP_000843.1:p.Ala122=