Canonical Allele Identifier: CA1814088353
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118110097G= , CM000670.2:g.118110097G= GRCh38
NC_000008.10:g.119122336G= , CM000670.1:g.119122336G= GRCh37
NC_000008.9:g.119191517G= NCBI36
NG_007455.2:g.6723C= , LRG_493:g.6723C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378204.7:c.950C= MANE Select ENSP00000367446.3:p.Thr317=
ENST00000436216.2:c.318C=
ENST00000378204.6:c.950C= ENSP00000367446.2:p.Thr317=
ENST00000436216.1:c.318C=
ENST00000437196.1:c.73+877C= ENSP00000407299.1:n.73+877C=
NM_000127.2:c.950C= , LRG_493t1:c.950C= NP_000118.2:p.Thr317=
NM_000127.3:c.950C= MANE Select NP_000118.2:p.Thr317=