Canonical Allele Identifier: CA1980214251
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584852_67584868delinsCCGCAGCCCTCTGGAGT , CM000673.2:g.67584852_67584868delinsCCGCAGCCCTCTGGAGT GRCh38
NC_000011.9:g.67352323_67352339delinsCCGCAGCCCTCTGGAGT , CM000673.1:g.67352323_67352339delinsCCGCAGCCCTCTGGAGT GRCh37
NC_000011.8:g.67108899_67108915delinsCCGCAGCCCTCTGGAGT NCBI36
NG_012075.1:g.6258_6274delinsCCGCAGCCCTCTGGAGT , LRG_723:g.6258_6274delinsCCGCAGCCCTCTGGAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.232+80_232+96delinsCCGCAGCCCTCTGGAGT ENSP00000381604.1:n.232+80_232+96delinsCCGCAGCCCTCTGGAGT
ENST00000398606.10:c.232+80_232+96delinsCCGCAGCCCTCTGGAGT MANE Select ENSP00000381607.3:n.232+80_232+96delinsCCGCAGCCCTCTGGAGT
ENST00000646888.1:c.125+80_125+96delinsCCGCAGCCCTCTGGAGT ENSP00000494477.1:n.125+80_125+96delinsCCGCAGCCCTCTGGAGT
ENST00000398603.5:c.232+80_232+96delinsCCGCAGCCCTCTGGAGT ENSP00000381604.1:n.232+80_232+96delinsCCGCAGCCCTCTGGAGT
ENST00000398606.7:c.232+80_232+96delinsCCGCAGCCCTCTGGAGT ENSP00000381607.3:n.232+80_232+96delinsCCGCAGCCCTCTGGAGT
ENST00000467591.1:n.58_74delinsCCGCAGCCCTCTGGAGT
ENST00000489040.1:n.311_327delinsCCGCAGCCCTCTGGAGT
ENST00000494593.1:n.742_758delinsCCGCAGCCCTCTGGAGT
ENST00000498765.5:c.195+80_195+96delinsCCGCAGCCCTCTGGAGT
NM_000852.3:c.232+80_232+96delinsCCGCAGCCCTCTGGAGT , LRG_723t1:c.232+80_232+96delinsCCGCAGCCCTCTGGAGT NP_000843.1:n.232+80_232+96delinsCCGCAGCCCTCTGGAGT
NM_000852.4:c.232+80_232+96delinsCCGCAGCCCTCTGGAGT MANE Select NP_000843.1:n.232+80_232+96delinsCCGCAGCCCTCTGGAGT