Canonical Allele Identifier: CA1967876051

Gene: EXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44108134A= , CM000673.2:g.44108134A=	GRCh38
NC_000011.9:g.44129684A= , CM000673.1:g.44129684A=	GRCh37
NC_000011.8:g.44086260A=	NCBI36
NG_007560.1:g.17586A= , LRG_494:g.17586A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343631.4:c.422A=	ENSP00000342656.3:p.Asp141=
ENST00000395673.8:c.422A=	ENSP00000379032.4:p.Asp141=
ENST00000531161.6:n.581A=
ENST00000682359.1:c.422A=	ENSP00000508226.1:p.Asp141=
ENST00000682711.1:c.-544+12282A=	ENSP00000506803.1:n.-544+12282A=
ENST00000682815.1:c.422A=	ENSP00000507234.1:p.Asp141=
ENST00000682947.1:n.596A=
ENST00000682993.1:c.422A=	ENSP00000507580.1:p.Asp141=
ENST00000683000.1:c.422A=	ENSP00000508361.1:p.Asp141=
ENST00000683299.1:n.839A=
ENST00000683870.1:c.422A=	ENSP00000507922.1:p.Asp141=
ENST00000683881.1:n.2983A=
ENST00000684039.1:c.422A=	ENSP00000507677.1:p.Asp141=
ENST00000684124.1:c.422A=	ENSP00000508332.1:p.Asp141=
ENST00000684533.1:c.422A=	ENSP00000507915.1:p.Asp141=
ENST00000533608.7:c.422A= MANE Select	ENSP00000431173.2:p.Asp141=
ENST00000343631.3:c.422A=	ENSP00000342656.3:p.Asp141=
ENST00000358681.8:c.422A=	ENSP00000351509.4:p.Asp141=
ENST00000395673.7:c.521A=	ENSP00000379032.3:p.Asp174=
ENST00000529186.1:n.120A=
ENST00000533608.5:c.422A=	ENSP00000431173.1:p.Asp141=
NM_000401.3:c.521A= , LRG_494t1:c.521A=	NP_000392.3:p.Asp174=
NM_001178083.1:c.422A=	NP_001171554.1:p.Asp141=
NM_207122.1:c.422A= , LRG_494t2:c.422A=	NP_997005.1:p.Asp141=
XM_011519950.1:c.560A=	XP_011518252.1:p.Asp187=
XM_011519951.1:c.461A=	XP_011518253.1:p.Asp154=
XM_024448383.1:c.560A=	XP_024304151.1:p.Asp187=
NM_001178083.2:c.422A=	NP_001171554.1:p.Asp141=
NM_207122.2:c.422A= MANE Select	NP_997005.1:p.Asp141=
NM_001178083.3:c.422A=	NP_001171554.1:p.Asp141=
NM_001389628.1:c.422A=	NP_001376557.1:p.Asp141=
NM_001389630.1:c.422A=	NP_001376559.1:p.Asp141=