Canonical Allele Identifier: CA1813950014
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117820086G= , CM000670.2:g.117820086G= GRCh38
NC_000008.10:g.118832325G= , CM000670.1:g.118832325G= GRCh37
NC_000008.9:g.118901506G= NCBI36
NG_007455.2:g.296734C= , LRG_493:g.296734C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684189.1:n.885-292C=
ENST00000378204.7:c.1418-292C= MANE Select ENSP00000367446.3:n.1418-292C=
ENST00000378204.6:c.1418-292C= ENSP00000367446.2:n.1418-292C=
ENST00000437196.1:c.*309-292C= ENSP00000407299.1:n.*309-292C=
NM_000127.2:c.1418-292C= , LRG_493t1:c.1418-292C= NP_000118.2:n.1418-292C=
NM_000127.3:c.1418-292C= MANE Select NP_000118.2:n.1418-292C=