Canonical Allele Identifier: CA1967883531

Gene: EXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44126931T= , CM000673.2:g.44126931T=	GRCh38
NC_000011.9:g.44148481T= , CM000673.1:g.44148481T=	GRCh37
NC_000011.8:g.44105057T=	NCBI36
NG_007560.1:g.36383T= , LRG_494:g.36383T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343631.4:c.1055T=	ENSP00000342656.3:p.Phe352=
ENST00000395673.8:c.1055T=	ENSP00000379032.4:p.Phe352=
ENST00000531161.6:n.1214T=
ENST00000682359.1:c.939+1947T=	ENSP00000508226.1:n.939+1947T=
ENST00000682711.1:c.-544+31079T=	ENSP00000506803.1:n.-544+31079T=
ENST00000682815.1:c.1055T=	ENSP00000507234.1:p.Phe352=
ENST00000682947.1:n.1229T=
ENST00000682993.1:c.1055T=	ENSP00000507580.1:p.Phe352=
ENST00000683000.1:c.1055T=	ENSP00000508361.1:p.Phe352=
ENST00000683299.1:n.1472T=
ENST00000683870.1:c.1055T=	ENSP00000507922.1:p.Phe352=
ENST00000683881.1:n.3616T=
ENST00000684039.1:c.1055T=	ENSP00000507677.1:p.Phe352=
ENST00000684124.1:c.1055T=	ENSP00000508332.1:p.Phe352=
ENST00000684533.1:c.744-3114T=	ENSP00000507915.1:n.744-3114T=
ENST00000533608.7:c.1055T= MANE Select	ENSP00000431173.2:p.Phe352=
ENST00000343631.3:c.1055T=	ENSP00000342656.3:p.Phe352=
ENST00000358681.8:c.1055T=	ENSP00000351509.4:p.Phe352=
ENST00000395673.7:c.1154T=	ENSP00000379032.3:p.Phe385=
ENST00000525559.1:n.29T=
ENST00000531161.5:n.232T=
ENST00000533608.5:c.1055T=	ENSP00000431173.1:p.Phe352=
NM_000401.3:c.1154T= , LRG_494t1:c.1154T=	NP_000392.3:p.Phe385=
NM_001178083.1:c.1055T=	NP_001171554.1:p.Phe352=
NM_207122.1:c.1055T= , LRG_494t2:c.1055T=	NP_997005.1:p.Phe352=
XM_011519950.1:c.1193T=	XP_011518252.1:p.Phe398=
XM_011519951.1:c.1094T=	XP_011518253.1:p.Phe365=
XM_024448383.1:c.1193T=	XP_024304151.1:p.Phe398=
NM_001178083.2:c.1055T=	NP_001171554.1:p.Phe352=
NM_207122.2:c.1055T= MANE Select	NP_997005.1:p.Phe352=
NM_001178083.3:c.1055T=	NP_001171554.1:p.Phe352=
NM_001389628.1:c.1055T=	NP_001376557.1:p.Phe352=
NM_001389630.1:c.1055T=	NP_001376559.1:p.Phe352=