Canonical Allele Identifier: CA1814090742
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111700_118111722delinsCGGCGGCGGCGGCGGCGCTGGGT , CM000670.2:g.118111700_118111722delinsCGGCGGCGGCGGCGGCGCTGGGT GRCh38
NC_000008.10:g.119123939_119123961delinsCGGCGGCGGCGGCGGCGCTGGGT , CM000670.1:g.119123939_119123961delinsCGGCGGCGGCGGCGGCGCTGGGT GRCh37
NC_000008.9:g.119193120_119193142delinsCGGCGGCGGCGGCGGCGCTGGGT NCBI36
NG_007455.2:g.5098_5120delinsACCCAGCGCCGCCGCCGCCGCCG , LRG_493:g.5098_5120delinsACCCAGCGCCGCCGCCGCCGCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000378204.7:c.-676_-654delinsACCCAGCGCCGCCGCCGCCGCCG MANE Select ENSP00000367446.3:n.-676_-654delinsACCCAGCGCCGCCGCCGCCGCCG
ENST00000378204.6:c.-676_-654delinsACCCAGCGCCGCCGCCGCCGCCG ENSP00000367446.2:n.-676_-654delinsACCCAGCGCCGCCGCCGCCGCCG
NM_000127.2:c.-676_-654delinsACCCAGCGCCGCCGCCGCCGCCG , LRG_493t1:c.-676_-654delinsACCCAGCGCCGCCGCCGCCGCCG NP_000118.2:n.-676_-654delinsACCCAGCGCCGCCGCCGCCGCCG
NM_000127.3:c.-676_-654delinsACCCAGCGCCGCCGCCGCCGCCG MANE Select NP_000118.2:n.-676_-654delinsACCCAGCGCCGCCGCCGCCGCCG