Canonical Allele Identifier: CA2614645993
Gene: GSTP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585199_67585200insTTTTTTAATGAGACGGC , CM000673.2:g.67585199_67585200insTTTTTTAATGAGACGGC GRCh38
NC_000011.9:g.67352670_67352671insTTTTTTAATGAGACGGC , CM000673.1:g.67352670_67352671insTTTTTTAATGAGACGGC GRCh37
NC_000011.8:g.67109246_67109247insTTTTTTAATGAGACGGC NCBI36
NG_012075.1:g.6605_6606insTTTTTTAATGAGACGGC , LRG_723:g.6605_6606insTTTTTTAATGAGACGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.294_295insTTTTTTAATGAGACGGC ENSP00000381604.1:p.Asp99PhefsTer33
ENST00000398606.10:c.294_295insTTTTTTAATGAGACGGC MANE Select ENSP00000381607.3:p.Asp99PhefsTer28
ENST00000646888.1:c.*10_*11insTTTTTTAATGAGACGGC ENSP00000494477.1:n.*10_*11insTTTTTTAATGAGACGGC
ENST00000398603.5:c.294_295insTTTTTTAATGAGACGGC ENSP00000381604.1:p.Asp99PhefsTer33
ENST00000398606.7:c.294_295insTTTTTTAATGAGACGGC ENSP00000381607.3:p.Asp99PhefsTer28
ENST00000467591.1:n.405_406insTTTTTTAATGAGACGGC
ENST00000494593.1:n.1089_1090insTTTTTTAATGAGACGGC
ENST00000498765.5:c.357_358insTTTTTTAATGAGACGGC
NM_000852.3:c.294_295insTTTTTTAATGAGACGGC , LRG_723t1:c.294_295insTTTTTTAATGAGACGGC NP_000843.1:p.Asp99PhefsTer28
NM_000852.4:c.294_295insTTTTTTAATGAGACGGC MANE Select NP_000843.1:p.Asp99PhefsTer28