Canonical Allele Identifier: CA1140583810

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21852751C= , CM000663.2:g.21852751C=	GRCh38
NC_000001.10:g.22179244C= , CM000663.1:g.22179244C=	GRCh37
NC_000001.9:g.22051831C=	NCBI36
NG_016740.1:g.89507G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.6673G= MANE Select	ENSP00000363827.3:p.Gly2225=
ENST00000374695.7:c.6673G=	ENSP00000363827.3:p.Gly2225=
ENST00000493940.2:n.304+213G=
NM_001291860.1:c.6676G=	NP_001278789.1:p.Gly2226=
NM_005529.6:c.6673G=	NP_005520.4:p.Gly2225=
XM_006710594.2:c.7219G=	XP_006710657.1:p.Gly2407=
XM_006710595.2:c.7171G=	XP_006710658.1:p.Gly2391=
XM_006710596.2:c.7150G=	XP_006710659.1:p.Gly2384=
XM_006710597.2:c.6673G=	XP_006710660.1:p.Gly2225=
XM_011541317.1:c.7222G=	XP_011539619.1:p.Gly2408=
XM_011541318.1:c.7222G=	XP_011539620.1:p.Gly2408=
XM_011541319.1:c.7222G=	XP_011539621.1:p.Gly2408=
XM_011541320.1:c.7140+168G=	XP_011539622.1:n.7140+168G=
XM_011541321.1:c.6727G=	XP_011539623.1:p.Gly2243=
XM_011541322.1:c.7222G=	XP_011539624.1:p.Gly2408=
XM_011541318.2:c.7222G=	XP_011539620.1:p.Gly2408=
XM_017001120.1:c.6868G=	XP_016856609.1:p.Gly2290=
XM_017001121.1:c.6817G=	XP_016856610.1:p.Gly2273=
XM_017001122.1:c.6814G=	XP_016856611.1:p.Gly2272=
NM_005529.7:c.6673G= MANE Select	NP_005520.4:p.Gly2225=
NM_001291860.2:c.6676G=	NP_001278789.1:p.Gly2226=