Canonical Allele Identifier: CA1139921392

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21833550C= , CM000663.2:g.21833550C=	GRCh38
NC_000001.10:g.22160043C= , CM000663.1:g.22160043C=	GRCh37
NC_000001.9:g.22032630C=	NCBI36
NG_016740.1:g.108708G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005529.7:c.10895G= MANE Select	NP_005520.4:p.Arg3632=
ENST00000374695.8:c.10895G= MANE Select	ENSP00000363827.3:p.Arg3632=
NM_001291860.1:c.10898G=	NP_001278789.1:p.Arg3633=
NM_001291860.2:c.10898G=	NP_001278789.1:p.Arg3633=
NM_005529.6:c.10895G=	NP_005520.4:p.Arg3632=
ENST00000374695.7:c.10895G=	ENSP00000363827.3:p.Arg3632=
ENST00000471322.2:n.1250G=
ENST00000635682.1:c.28G=
XM_006710594.2:c.11441G=	XP_006710657.1:p.Arg3814=
XM_006710595.2:c.11393G=	XP_006710658.1:p.Arg3798=
XM_006710596.2:c.11372G=	XP_006710659.1:p.Arg3791=
XM_006710597.2:c.10895G=	XP_006710660.1:p.Arg3632=
XM_011541317.1:c.11444G=	XP_011539619.1:p.Arg3815=
XM_011541318.1:c.11444G=	XP_011539620.1:p.Arg3815=
XM_011541318.2:c.11444G=	XP_011539620.1:p.Arg3815=
XM_011541319.1:c.11444G=	XP_011539621.1:p.Arg3815=
XM_011541320.1:c.11165G=	XP_011539622.1:p.Arg3722=
XM_011541321.1:c.10949G=	XP_011539623.1:p.Arg3650=
XM_017001120.1:c.11090G=	XP_016856609.1:p.Arg3697=
XM_017001121.1:c.11039G=	XP_016856610.1:p.Arg3680=
XM_017001122.1:c.11036G=	XP_016856611.1:p.Arg3679=