Canonical Allele Identifier: CA1814088351
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118110096G= , CM000670.2:g.118110096G= GRCh38
NC_000008.10:g.119122335G= , CM000670.1:g.119122335G= GRCh37
NC_000008.9:g.119191516G= NCBI36
NG_007455.2:g.6724C= , LRG_493:g.6724C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.951C= MANE Select ENSP00000367446.3:p.Thr317=
ENST00000436216.2:c.319C=
ENST00000378204.6:c.951C= ENSP00000367446.2:p.Thr317=
ENST00000436216.1:c.319C=
ENST00000437196.1:c.73+878C= ENSP00000407299.1:n.73+878C=
NM_000127.2:c.951C= , LRG_493t1:c.951C= NP_000118.2:p.Thr317=
NM_000127.3:c.951C= MANE Select NP_000118.2:p.Thr317=