Canonical Allele Identifier: CA381522128
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586270A>T , CM000673.2:g.67586270A>T GRCh38
NC_000011.9:g.67353741A>T , CM000673.1:g.67353741A>T GRCh37
NC_000011.8:g.67110317A>T NCBI36
NG_012075.1:g.7676A>T , LRG_723:g.7676A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-119A>T ENSP00000381604.1:n.337-119A>T
ENST00000398606.10:c.444+59A>T MANE Select ENSP00000381607.3:n.444+59A>T
ENST00000646888.1:c.*160+59A>T ENSP00000494477.1:n.*160+59A>T
ENST00000398603.5:c.337-119A>T ENSP00000381604.1:n.337-119A>T
ENST00000398606.7:c.444+59A>T ENSP00000381607.3:n.444+59A>T
ENST00000467591.1:n.555+59A>T
ENST00000494593.1:n.1298A>T
ENST00000495996.1:c.167A>T ENSP00000484686.1:p.Gln56Leu
ENST00000498765.5:c.507+59A>T
NM_000852.3:c.444+59A>T , LRG_723t1:c.444+59A>T NP_000843.1:n.444+59A>T
NM_000852.4:c.444+59A>T MANE Select NP_000843.1:n.444+59A>T