Canonical Allele Identifier: CA381521656
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586218A>G , CM000673.2:g.67586218A>G GRCh38
NC_000011.9:g.67353689A>G , CM000673.1:g.67353689A>G GRCh37
NC_000011.8:g.67110265A>G NCBI36
NG_012075.1:g.7624A>G , LRG_723:g.7624A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-171A>G ENSP00000381604.1:n.337-171A>G
ENST00000398606.10:c.444+7A>G MANE Select ENSP00000381607.3:n.444+7A>G
ENST00000646888.1:c.*160+7A>G ENSP00000494477.1:n.*160+7A>G
ENST00000398603.5:c.337-171A>G ENSP00000381604.1:n.337-171A>G
ENST00000398606.7:c.444+7A>G ENSP00000381607.3:n.444+7A>G
ENST00000467591.1:n.555+7A>G
ENST00000494593.1:n.1246A>G
ENST00000495996.1:c.115A>G ENSP00000484686.1:p.Ile39Val
ENST00000498765.5:c.507+7A>G
NM_000852.3:c.444+7A>G , LRG_723t1:c.444+7A>G NP_000843.1:n.444+7A>G
NM_000852.4:c.444+7A>G MANE Select NP_000843.1:n.444+7A>G