Canonical Allele Identifier: CA381520718
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586135T>G , CM000673.2:g.67586135T>G GRCh38
NC_000011.9:g.67353606T>G , CM000673.1:g.67353606T>G GRCh37
NC_000011.8:g.67110182T>G NCBI36
NG_012075.1:g.7541T>G , LRG_723:g.7541T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-254T>G ENSP00000381604.1:n.337-254T>G
ENST00000398606.10:c.368T>G MANE Select ENSP00000381607.3:p.Leu123Arg
ENST00000646888.1:c.*84T>G ENSP00000494477.1:n.*84T>G
ENST00000398603.5:c.337-254T>G ENSP00000381604.1:n.337-254T>G
ENST00000398606.7:c.368T>G ENSP00000381607.3:p.Leu123Arg
ENST00000467591.1:n.479T>G
ENST00000494593.1:n.1163T>G
ENST00000495996.1:c.32T>G ENSP00000484686.1:p.Leu11Arg
ENST00000498765.5:c.431T>G
NM_000852.3:c.368T>G , LRG_723t1:c.368T>G NP_000843.1:p.Leu123Arg
NM_000852.4:c.368T>G MANE Select NP_000843.1:p.Leu123Arg