Canonical Allele Identifier: CA670563

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21842135C>T , CM000663.2:g.21842135C>T	GRCh38
NC_000001.10:g.22168628C>T , CM000663.1:g.22168628C>T	GRCh37
NC_000001.9:g.22041215C>T	NCBI36
NG_016740.1:g.100123G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.9060G>A MANE Select	ENSP00000363827.3:p.Arg3020=
ENST00000374695.7:c.9060G>A	ENSP00000363827.3:p.Arg3020=
NM_001291860.1:c.9063G>A	NP_001278789.1:p.Arg3021=
NM_005529.6:c.9060G>A	NP_005520.4:p.Arg3020=
XM_006710594.2:c.9606G>A	XP_006710657.1:p.Arg3202=
XM_006710595.2:c.9558G>A	XP_006710658.1:p.Arg3186=
XM_006710596.2:c.9537G>A	XP_006710659.1:p.Arg3179=
XM_006710597.2:c.9060G>A	XP_006710660.1:p.Arg3020=
XM_011541317.1:c.9609G>A	XP_011539619.1:p.Arg3203=
XM_011541318.1:c.9609G>A	XP_011539620.1:p.Arg3203=
XM_011541319.1:c.9609G>A	XP_011539621.1:p.Arg3203=
XM_011541320.1:c.9330G>A	XP_011539622.1:p.Arg3110=
XM_011541321.1:c.9114G>A	XP_011539623.1:p.Arg3038=
XM_011541318.2:c.9609G>A	XP_011539620.1:p.Arg3203=
XM_017001120.1:c.9255G>A	XP_016856609.1:p.Arg3085=
XM_017001121.1:c.9204G>A	XP_016856610.1:p.Arg3068=
XM_017001122.1:c.9201G>A	XP_016856611.1:p.Arg3067=
NM_005529.7:c.9060G>A MANE Select	NP_005520.4:p.Arg3020=
NM_001291860.2:c.9063G>A	NP_001278789.1:p.Arg3021=