Canonical Allele Identifier: CA669987

Gene: HSPG2

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.10895G>A MANE Select	ENSP00000363827.3:p.Arg3632Gln
ENST00000374695.7:c.10895G>A	ENSP00000363827.3:p.Arg3632Gln
ENST00000471322.2:n.1250G>A
ENST00000635682.1:c.28G>A
NM_001291860.1:c.10898G>A	NP_001278789.1:p.Arg3633Gln
NM_005529.6:c.10895G>A	NP_005520.4:p.Arg3632Gln
XM_006710594.2:c.11441G>A	XP_006710657.1:p.Arg3814Gln
XM_006710595.2:c.11393G>A	XP_006710658.1:p.Arg3798Gln
XM_006710596.2:c.11372G>A	XP_006710659.1:p.Arg3791Gln
XM_006710597.2:c.10895G>A	XP_006710660.1:p.Arg3632Gln
XM_011541317.1:c.11444G>A	XP_011539619.1:p.Arg3815Gln
XM_011541318.1:c.11444G>A	XP_011539620.1:p.Arg3815Gln
XM_011541319.1:c.11444G>A	XP_011539621.1:p.Arg3815Gln
XM_011541320.1:c.11165G>A	XP_011539622.1:p.Arg3722Gln
XM_011541321.1:c.10949G>A	XP_011539623.1:p.Arg3650Gln
XM_011541318.2:c.11444G>A	XP_011539620.1:p.Arg3815Gln
XM_017001120.1:c.11090G>A	XP_016856609.1:p.Arg3697Gln
XM_017001121.1:c.11039G>A	XP_016856610.1:p.Arg3680Gln
XM_017001122.1:c.11036G>A	XP_016856611.1:p.Arg3679Gln
NM_005529.7:c.10895G>A MANE Select	NP_005520.4:p.Arg3632Gln
NM_001291860.2:c.10898G>A	NP_001278789.1:p.Arg3633Gln