Canonical Allele Identifier: CA1813957394
Gene: EXT1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000684189.1:n.479C=
ENST00000378204.7:c.1012C= MANE Select ENSP00000367446.3:p.Arg338=
ENST00000436216.2:c.380C=
ENST00000378204.6:c.1012C= ENSP00000367446.2:p.Arg338=
ENST00000436216.1:c.380C=
ENST00000437196.1:c.74-1601C= ENSP00000407299.1:n.74-1601C=
NM_000127.2:c.1012C= , LRG_493t1:c.1012C= NP_000118.2:p.Arg338=
NM_000127.3:c.1012C= MANE Select NP_000118.2:p.Arg338=