Canonical Allele Identifier: CA670404

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21839991C>T , CM000663.2:g.21839991C>T	GRCh38
NC_000001.10:g.22166484C>T , CM000663.1:g.22166484C>T	GRCh37
NC_000001.9:g.22039071C>T	NCBI36
NG_016740.1:g.102267G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.9540G>A MANE Select	ENSP00000363827.3:p.Ala3180=
ENST00000374695.7:c.9540G>A	ENSP00000363827.3:p.Ala3180=
NM_001291860.1:c.9543G>A	NP_001278789.1:p.Ala3181=
NM_005529.6:c.9540G>A	NP_005520.4:p.Ala3180=
XM_006710594.2:c.10086G>A	XP_006710657.1:p.Ala3362=
XM_006710595.2:c.10038G>A	XP_006710658.1:p.Ala3346=
XM_006710596.2:c.10017G>A	XP_006710659.1:p.Ala3339=
XM_006710597.2:c.9540G>A	XP_006710660.1:p.Ala3180=
XM_011541317.1:c.10089G>A	XP_011539619.1:p.Ala3363=
XM_011541318.1:c.10089G>A	XP_011539620.1:p.Ala3363=
XM_011541319.1:c.10089G>A	XP_011539621.1:p.Ala3363=
XM_011541320.1:c.9810G>A	XP_011539622.1:p.Ala3270=
XM_011541321.1:c.9594G>A	XP_011539623.1:p.Ala3198=
XM_011541318.2:c.10089G>A	XP_011539620.1:p.Ala3363=
XM_017001120.1:c.9735G>A	XP_016856609.1:p.Ala3245=
XM_017001121.1:c.9684G>A	XP_016856610.1:p.Ala3228=
XM_017001122.1:c.9681G>A	XP_016856611.1:p.Ala3227=
NM_005529.7:c.9540G>A MANE Select	NP_005520.4:p.Ala3180=
NM_001291860.2:c.9543G>A	NP_001278789.1:p.Ala3181=