Canonical Allele Identifier: CA670747

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21844220G>A , CM000663.2:g.21844220G>A	GRCh38
NC_000001.10:g.22170713G>A , CM000663.1:g.22170713G>A	GRCh37
NC_000001.9:g.22043300G>A	NCBI36
NG_016740.1:g.98038C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.8544C>T MANE Select	ENSP00000363827.3:p.Cys2848=
ENST00000374695.7:c.8544C>T	ENSP00000363827.3:p.Cys2848=
NM_001291860.1:c.8547C>T	NP_001278789.1:p.Cys2849=
NM_005529.6:c.8544C>T	NP_005520.4:p.Cys2848=
XM_006710594.2:c.9090C>T	XP_006710657.1:p.Cys3030=
XM_006710595.2:c.9042C>T	XP_006710658.1:p.Cys3014=
XM_006710596.2:c.9021C>T	XP_006710659.1:p.Cys3007=
XM_006710597.2:c.8544C>T	XP_006710660.1:p.Cys2848=
XM_011541317.1:c.9093C>T	XP_011539619.1:p.Cys3031=
XM_011541318.1:c.9093C>T	XP_011539620.1:p.Cys3031=
XM_011541319.1:c.9093C>T	XP_011539621.1:p.Cys3031=
XM_011541320.1:c.8814C>T	XP_011539622.1:p.Cys2938=
XM_011541321.1:c.8598C>T	XP_011539623.1:p.Cys2866=
XM_011541318.2:c.9093C>T	XP_011539620.1:p.Cys3031=
XM_017001120.1:c.8739C>T	XP_016856609.1:p.Cys2913=
XM_017001121.1:c.8688C>T	XP_016856610.1:p.Cys2896=
XM_017001122.1:c.8685C>T	XP_016856611.1:p.Cys2895=
NM_005529.7:c.8544C>T MANE Select	NP_005520.4:p.Cys2848=
NM_001291860.2:c.8547C>T	NP_001278789.1:p.Cys2849=