Canonical Allele Identifier: CA1813950001
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117820051G= , CM000670.2:g.117820051G= GRCh38
NC_000008.10:g.118832290G= , CM000670.1:g.118832290G= GRCh37
NC_000008.9:g.118901471G= NCBI36
NG_007455.2:g.296769C= , LRG_493:g.296769C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684189.1:n.885-257C=
ENST00000378204.7:c.1418-257C= MANE Select ENSP00000367446.3:n.1418-257C=
ENST00000378204.6:c.1418-257C= ENSP00000367446.2:n.1418-257C=
ENST00000437196.1:c.*309-257C= ENSP00000407299.1:n.*309-257C=
NM_000127.2:c.1418-257C= , LRG_493t1:c.1418-257C= NP_000118.2:n.1418-257C=
NM_000127.3:c.1418-257C= MANE Select NP_000118.2:n.1418-257C=