Canonical Allele Identifier: CA1813956706
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117835519T= , CM000670.2:g.117835519T= GRCh38
NC_000008.10:g.118847758T= , CM000670.1:g.118847758T= GRCh37
NC_000008.9:g.118916939T= NCBI36
NG_007455.2:g.281301A= , LRG_493:g.281301A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684189.1:n.556A=
ENST00000378204.7:c.1089A= MANE Select ENSP00000367446.3:p.Gly363=
ENST00000436216.2:c.457A=
ENST00000378204.6:c.1089A= ENSP00000367446.2:p.Gly363=
ENST00000436216.1:c.457A=
ENST00000437196.1:c.106A= ENSP00000407299.1:p.Met36=
NM_000127.2:c.1089A= , LRG_493t1:c.1089A= NP_000118.2:p.Gly363=
NM_000127.3:c.1089A= MANE Select NP_000118.2:p.Gly363=