Canonical Allele Identifier: CA1814088269

Gene: EXT1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118110049G= , CM000670.2:g.118110049G=	GRCh38
NC_000008.10:g.119122288G= , CM000670.1:g.119122288G=	GRCh37
NC_000008.9:g.119191469G=	NCBI36
NG_007455.2:g.6771C= , LRG_493:g.6771C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378204.7:c.962+36C= MANE Select	ENSP00000367446.3:n.962+36C=
ENST00000436216.2:c.330+36C=
ENST00000378204.6:c.962+36C=	ENSP00000367446.2:n.962+36C=
ENST00000436216.1:c.330+36C=
ENST00000437196.1:c.73+925C=	ENSP00000407299.1:n.73+925C=
NM_000127.2:c.962+36C= , LRG_493t1:c.962+36C=	NP_000118.2:n.962+36C=
NM_000127.3:c.962+36C= MANE Select	NP_000118.2:n.962+36C=