Canonical Allele Identifier: CA19113331

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21846692C>T , CM000663.2:g.21846692C>T	GRCh38
NC_000001.10:g.22173185C>T , CM000663.1:g.22173185C>T	GRCh37
NC_000001.9:g.22045772C>T	NCBI36
NG_016740.1:g.95566G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.8165-93G>A MANE Select	ENSP00000363827.3:n.8165-93G>A
ENST00000374695.7:c.8165-93G>A	ENSP00000363827.3:n.8165-93G>A
ENST00000453796.1:n.410-93G>A
NM_001291860.1:c.8168-93G>A	NP_001278789.1:n.8168-93G>A
NM_005529.6:c.8165-93G>A	NP_005520.4:n.8165-93G>A
XM_006710594.2:c.8711-93G>A	XP_006710657.1:n.8711-93G>A
XM_006710595.2:c.8663-93G>A	XP_006710658.1:n.8663-93G>A
XM_006710596.2:c.8642-93G>A	XP_006710659.1:n.8642-93G>A
XM_006710597.2:c.8165-93G>A	XP_006710660.1:n.8165-93G>A
XM_011541317.1:c.8714-93G>A	XP_011539619.1:n.8714-93G>A
XM_011541318.1:c.8714-93G>A	XP_011539620.1:n.8714-93G>A
XM_011541319.1:c.8714-93G>A	XP_011539621.1:n.8714-93G>A
XM_011541320.1:c.8435-93G>A	XP_011539622.1:n.8435-93G>A
XM_011541321.1:c.8219-93G>A	XP_011539623.1:n.8219-93G>A
XM_011541318.2:c.8714-93G>A	XP_011539620.1:n.8714-93G>A
XM_017001120.1:c.8360-93G>A	XP_016856609.1:n.8360-93G>A
XM_017001121.1:c.8309-93G>A	XP_016856610.1:n.8309-93G>A
XM_017001122.1:c.8306-93G>A	XP_016856611.1:n.8306-93G>A
NM_005529.7:c.8165-93G>A MANE Select	NP_005520.4:n.8165-93G>A
NM_001291860.2:c.8168-93G>A	NP_001278789.1:n.8168-93G>A