Canonical Allele Identifier: CA1967882681

Gene: EXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44124963C= , CM000673.2:g.44124963C=	GRCh38
NC_000011.9:g.44146513C= , CM000673.1:g.44146513C=	GRCh37
NC_000011.8:g.44103089C=	NCBI36
NG_007560.1:g.34415C= , LRG_494:g.34415C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343631.4:c.918C=	ENSP00000342656.3:p.Phe306=
ENST00000395673.8:c.918C=	ENSP00000379032.4:p.Phe306=
ENST00000531161.6:n.1077C=
ENST00000682359.1:c.918C=	ENSP00000508226.1:p.Phe306=
ENST00000682711.1:c.-544+29111C=	ENSP00000506803.1:n.-544+29111C=
ENST00000682815.1:c.918C=	ENSP00000507234.1:p.Phe306=
ENST00000682947.1:n.1092C=
ENST00000682993.1:c.918C=	ENSP00000507580.1:p.Phe306=
ENST00000683000.1:c.918C=	ENSP00000508361.1:p.Phe306=
ENST00000683299.1:n.1335C=
ENST00000683870.1:c.918C=	ENSP00000507922.1:p.Phe306=
ENST00000683881.1:n.3479C=
ENST00000684039.1:c.918C=	ENSP00000507677.1:p.Phe306=
ENST00000684124.1:c.918C=	ENSP00000508332.1:p.Phe306=
ENST00000684533.1:c.744-5082C=	ENSP00000507915.1:n.744-5082C=
ENST00000533608.7:c.918C= MANE Select	ENSP00000431173.2:p.Phe306=
ENST00000343631.3:c.918C=	ENSP00000342656.3:p.Phe306=
ENST00000358681.8:c.918C=	ENSP00000351509.4:p.Phe306=
ENST00000395673.7:c.1017C=	ENSP00000379032.3:p.Phe339=
ENST00000531161.5:n.95C=
ENST00000533608.5:c.918C=	ENSP00000431173.1:p.Phe306=
NM_000401.3:c.1017C= , LRG_494t1:c.1017C=	NP_000392.3:p.Phe339=
NM_001178083.1:c.918C=	NP_001171554.1:p.Phe306=
NM_207122.1:c.918C= , LRG_494t2:c.918C=	NP_997005.1:p.Phe306=
XM_011519950.1:c.1056C=	XP_011518252.1:p.Phe352=
XM_011519951.1:c.957C=	XP_011518253.1:p.Phe319=
XM_024448383.1:c.1056C=	XP_024304151.1:p.Phe352=
NM_001178083.2:c.918C=	NP_001171554.1:p.Phe306=
NM_207122.2:c.918C= MANE Select	NP_997005.1:p.Phe306=
NM_001178083.3:c.918C=	NP_001171554.1:p.Phe306=
NM_001389628.1:c.918C=	NP_001376557.1:p.Phe306=
NM_001389630.1:c.918C=	NP_001376559.1:p.Phe306=