Canonical Allele Identifier: CA1814090731
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111697_118111725delinsAGGCGGCGGCGGCGGCGGCGCTGGGTGGC , CM000670.2:g.118111697_118111725delinsAGGCGGCGGCGGCGGCGGCGCTGGGTGGC GRCh38
NC_000008.10:g.119123936_119123964delinsAGGCGGCGGCGGCGGCGGCGCTGGGTGGC , CM000670.1:g.119123936_119123964delinsAGGCGGCGGCGGCGGCGGCGCTGGGTGGC GRCh37
NC_000008.9:g.119193117_119193145delinsAGGCGGCGGCGGCGGCGGCGCTGGGTGGC NCBI36
NG_007455.2:g.5095_5123delinsGCCACCCAGCGCCGCCGCCGCCGCCGCCT , LRG_493:g.5095_5123delinsGCCACCCAGCGCCGCCGCCGCCGCCGCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.-679_-651delinsGCCACCCAGCGCCGCCGCCGCCGCCGCCT MANE Select ENSP00000367446.3:n.-679_-651delinsGCCACCCAGCGCCGCCGCCGCCGCCG...
ENST00000378204.6:c.-679_-651delinsGCCACCCAGCGCCGCCGCCGCCGCCGCCT ENSP00000367446.2:n.-679_-651delinsGCCACCCAGCGCCGCCGCCGCCGCCG...
NM_000127.2:c.-679_-651delinsGCCACCCAGCGCCGCCGCCGCCGCCGCCT , LRG_493t1:c.-679_-651delinsGCCACCCAGCGCCGCCGCCGCCGCCGCCT NP_000118.2:n.-679_-651delinsGCCACCCAGCGCCGCCGCCGCCGCCGCCT
NM_000127.3:c.-679_-651delinsGCCACCCAGCGCCGCCGCCGCCGCCGCCT MANE Select NP_000118.2:n.-679_-651delinsGCCACCCAGCGCCGCCGCCGCCGCCGCCT