Canonical Allele Identifier: CA670273

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21839066C>T , CM000663.2:g.21839066C>T	GRCh38
NC_000001.10:g.22165559C>T , CM000663.1:g.22165559C>T	GRCh37
NC_000001.9:g.22038146C>T	NCBI36
NG_016740.1:g.103192G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.9909G>A MANE Select	ENSP00000363827.3:p.Thr3303=
ENST00000374695.7:c.9909G>A	ENSP00000363827.3:p.Thr3303=
NM_001291860.1:c.9912G>A	NP_001278789.1:p.Thr3304=
NM_005529.6:c.9909G>A	NP_005520.4:p.Thr3303=
XM_006710594.2:c.10455G>A	XP_006710657.1:p.Thr3485=
XM_006710595.2:c.10407G>A	XP_006710658.1:p.Thr3469=
XM_006710596.2:c.10386G>A	XP_006710659.1:p.Thr3462=
XM_006710597.2:c.9909G>A	XP_006710660.1:p.Thr3303=
XM_011541317.1:c.10458G>A	XP_011539619.1:p.Thr3486=
XM_011541318.1:c.10458G>A	XP_011539620.1:p.Thr3486=
XM_011541319.1:c.10458G>A	XP_011539621.1:p.Thr3486=
XM_011541320.1:c.10179G>A	XP_011539622.1:p.Thr3393=
XM_011541321.1:c.9963G>A	XP_011539623.1:p.Thr3321=
XM_011541318.2:c.10458G>A	XP_011539620.1:p.Thr3486=
XM_017001120.1:c.10104G>A	XP_016856609.1:p.Thr3368=
XM_017001121.1:c.10053G>A	XP_016856610.1:p.Thr3351=
XM_017001122.1:c.10050G>A	XP_016856611.1:p.Thr3350=
NM_005529.7:c.9909G>A MANE Select	NP_005520.4:p.Thr3303=
NM_001291860.2:c.9912G>A	NP_001278789.1:p.Thr3304=