Canonical Allele Identifier: CA10588283

Gene: HSPG2

Linked Data

• ClinVar Variation Id: 265454
• ClinVar RCV Id: RCV000254867 ; RCV002487170
• dbSNP Id: rs778653296
• gnomAD v2: 1-22178283-C-T
• gnomAD v4: 1-21851790-C-T
• COSMIC: COSM1295899
• MyVariant Identifiers: chr1:g.22178283C>T (hg19) ; chr1:g.21851790C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21851790C>T , CM000663.2:g.21851790C>T	GRCh38
NC_000001.10:g.22178283C>T , CM000663.1:g.22178283C>T	GRCh37
NC_000001.9:g.22050870C>T	NCBI36
NG_016740.1:g.90468G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.7006+1G>A MANE Select	ENSP00000363827.3:n.7006+1G>A
ENST00000374695.7:c.7006+1G>A	ENSP00000363827.3:n.7006+1G>A
ENST00000493940.2:n.305-200G>A
NM_001291860.1:c.7009+1G>A	NP_001278789.1:n.7009+1G>A
NM_005529.6:c.7006+1G>A	NP_005520.4:n.7006+1G>A
XM_006710594.2:c.7552+1G>A	XP_006710657.1:n.7552+1G>A
XM_006710595.2:c.7504+1G>A	XP_006710658.1:n.7504+1G>A
XM_006710596.2:c.7483+1G>A	XP_006710659.1:n.7483+1G>A
XM_006710597.2:c.7006+1G>A	XP_006710660.1:n.7006+1G>A
XM_011541317.1:c.7555+1G>A	XP_011539619.1:n.7555+1G>A
XM_011541318.1:c.7555+1G>A	XP_011539620.1:n.7555+1G>A
XM_011541319.1:c.7555+1G>A	XP_011539621.1:n.7555+1G>A
XM_011541320.1:c.7276+1G>A	XP_011539622.1:n.7276+1G>A
XM_011541321.1:c.7060+1G>A	XP_011539623.1:n.7060+1G>A
XM_011541322.1:c.7555+1G>A	XP_011539624.1:n.7555+1G>A
XM_011541318.2:c.7555+1G>A	XP_011539620.1:n.7555+1G>A
XM_017001120.1:c.7201+1G>A	XP_016856609.1:n.7201+1G>A
XM_017001121.1:c.7150+1G>A	XP_016856610.1:n.7150+1G>A
XM_017001122.1:c.7147+1G>A	XP_016856611.1:n.7147+1G>A
NM_005529.7:c.7006+1G>A MANE Select	NP_005520.4:n.7006+1G>A
NM_001291860.2:c.7009+1G>A	NP_001278789.1:n.7009+1G>A