Canonical Allele Identifier: CA1813956707
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117835521C= , CM000670.2:g.117835521C= GRCh38
NC_000008.10:g.118847760C= , CM000670.1:g.118847760C= GRCh37
NC_000008.9:g.118916941C= NCBI36
NG_007455.2:g.281299G= , LRG_493:g.281299G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684189.1:n.554G=
ENST00000378204.7:c.1087G= MANE Select ENSP00000367446.3:p.Gly363=
ENST00000436216.2:c.455G=
ENST00000378204.6:c.1087G= ENSP00000367446.2:p.Gly363=
ENST00000436216.1:c.455G=
ENST00000437196.1:c.104G= ENSP00000407299.1:p.Trp35=
NM_000127.2:c.1087G= , LRG_493t1:c.1087G= NP_000118.2:p.Gly363=
NM_000127.3:c.1087G= MANE Select NP_000118.2:p.Gly363=