Canonical Allele Identifier: CA670909

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21847366C>T , CM000663.2:g.21847366C>T	GRCh38
NC_000001.10:g.22173859C>T , CM000663.1:g.22173859C>T	GRCh37
NC_000001.9:g.22046446C>T	NCBI36
NG_016740.1:g.94892G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005529.7:c.8152G>A MANE Select	NP_005520.4:p.Gly2718Ser
ENST00000374695.8:c.8152G>A MANE Select	ENSP00000363827.3:p.Gly2718Ser
NM_001291860.1:c.8155G>A	NP_001278789.1:p.Gly2719Ser
NM_001291860.2:c.8155G>A	NP_001278789.1:p.Gly2719Ser
NM_005529.6:c.8152G>A	NP_005520.4:p.Gly2718Ser
ENST00000374695.7:c.8152G>A	ENSP00000363827.3:p.Gly2718Ser
ENST00000453796.1:n.397G>A
XM_006710594.2:c.8698G>A	XP_006710657.1:p.Gly2900Ser
XM_006710595.2:c.8650G>A	XP_006710658.1:p.Gly2884Ser
XM_006710596.2:c.8629G>A	XP_006710659.1:p.Gly2877Ser
XM_006710597.2:c.8152G>A	XP_006710660.1:p.Gly2718Ser
XM_011541317.1:c.8701G>A	XP_011539619.1:p.Gly2901Ser
XM_011541318.1:c.8701G>A	XP_011539620.1:p.Gly2901Ser
XM_011541318.2:c.8701G>A	XP_011539620.1:p.Gly2901Ser
XM_011541319.1:c.8701G>A	XP_011539621.1:p.Gly2901Ser
XM_011541320.1:c.8422G>A	XP_011539622.1:p.Gly2808Ser
XM_011541321.1:c.8206G>A	XP_011539623.1:p.Gly2736Ser
XM_017001120.1:c.8347G>A	XP_016856609.1:p.Gly2783Ser
XM_017001121.1:c.8296G>A	XP_016856610.1:p.Gly2766Ser
XM_017001122.1:c.8293G>A	XP_016856611.1:p.Gly2765Ser