Canonical Allele Identifier: CA2688347386
Gene: EXT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118111472A>T , CM000670.2:g.118111472A>T GRCh38
NC_000008.10:g.119123711A>T , CM000670.1:g.119123711A>T GRCh37
NC_000008.9:g.119192892A>T NCBI36
NG_007455.2:g.5348T>A , LRG_493:g.5348T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.-426T>A MANE Select ENSP00000367446.3:n.-426T>A
ENST00000378204.6:c.-426T>A ENSP00000367446.2:n.-426T>A
NM_000127.2:c.-426T>A , LRG_493t1:c.-426T>A NP_000118.2:n.-426T>A
NM_000127.3:c.-426T>A MANE Select NP_000118.2:n.-426T>A