Canonical Allele Identifier: CA2695210040
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117837152del , CM000670.2:g.117837152del GRCh38
NC_000008.10:g.118849391del , CM000670.1:g.118849391del GRCh37
NC_000008.9:g.118918572del NCBI36
NG_007455.2:g.279668del , LRG_493:g.279668del

Transcript Alleles

HGVS Amino-acid change
ENST00000684189.1:n.479del
ENST00000378204.7:c.1012del MANE Select ENSP00000367446.3:p.Arg338ValfsTer21
ENST00000436216.2:c.380del
ENST00000378204.6:c.1012del ENSP00000367446.2:p.Arg338ValfsTer21
ENST00000436216.1:c.380del
ENST00000437196.1:c.74-1601del ENSP00000407299.1:n.74-1601del
NM_000127.2:c.1012del , LRG_493t1:c.1012del NP_000118.2:p.Arg338ValfsTer21
NM_000127.3:c.1012del MANE Select NP_000118.2:p.Arg338ValfsTer21