Canonical Allele Identifier: CA1813915695

Gene: EXT1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117807261C= , CM000670.2:g.117807261C=	GRCh38
NC_000008.10:g.118819500C= , CM000670.1:g.118819500C=	GRCh37
NC_000008.9:g.118888681C=	NCBI36
NG_007455.2:g.309559G= , LRG_493:g.309559G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684189.1:n.1306G=
ENST00000378204.7:c.1839G= MANE Select	ENSP00000367446.3:p.Thr613=
ENST00000378204.6:c.1839G=	ENSP00000367446.2:p.Thr613=
ENST00000437196.1:c.*730G=	ENSP00000407299.1:n.*730G=
NM_000127.2:c.1839G= , LRG_493t1:c.1839G=	NP_000118.2:p.Thr613=
NM_000127.3:c.1839G= MANE Select	NP_000118.2:p.Thr613=