Canonical Allele Identifier: CA1813957416
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117837198A= , CM000670.2:g.117837198A= GRCh38
NC_000008.10:g.118849437A= , CM000670.1:g.118849437A= GRCh37
NC_000008.9:g.118918618A= NCBI36
NG_007455.2:g.279622T= , LRG_493:g.279622T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684189.1:n.433T=
ENST00000378204.7:c.966T= MANE Select ENSP00000367446.3:p.Tyr322=
ENST00000436216.2:c.334T=
ENST00000378204.6:c.966T= ENSP00000367446.2:p.Tyr322=
ENST00000436216.1:c.334T=
ENST00000437196.1:c.74-1647T= ENSP00000407299.1:n.74-1647T=
NM_000127.2:c.966T= , LRG_493t1:c.966T= NP_000118.2:p.Tyr322=
NM_000127.3:c.966T= MANE Select NP_000118.2:p.Tyr322=