Canonical Allele Identifier: CA673644

Gene: HSPG2

Linked Data

• ClinVar Variation Id: 295901
• ClinVar RCV Id: RCV000322882 ; RCV000372886 ; RCV002059444
• dbSNP Id: rs200930800
• ExAC: 1:22213899 C / T
• gnomAD v2: 1-22213899-C-T
• gnomAD v3: 1-21887406-C-T
• gnomAD v4: 1-21887406-C-T
• MyVariant Identifiers: chr1:g.22213899C>T (hg19) ; chr1:g.21887406C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21887406C>T , CM000663.2:g.21887406C>T	GRCh38
NC_000001.10:g.22213899C>T , CM000663.1:g.22213899C>T	GRCh37
NC_000001.9:g.22086486C>T	NCBI36
NG_016740.1:g.54852G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374673.4:c.765+14G>A
ENST00000374695.8:c.958+14G>A MANE Select	ENSP00000363827.3:n.958+14G>A
ENST00000374673.3:n.438+14G>A
ENST00000374695.7:c.958+14G>A	ENSP00000363827.3:n.958+14G>A
ENST00000412328.5:n.726+14G>A
NM_001291860.1:c.958+14G>A	NP_001278789.1:n.958+14G>A
NM_005529.6:c.958+14G>A	NP_005520.4:n.958+14G>A
XM_006710594.2:c.1009+14G>A	XP_006710657.1:n.1009+14G>A
XM_006710595.2:c.958+14G>A	XP_006710658.1:n.958+14G>A
XM_006710596.2:c.1009+14G>A	XP_006710659.1:n.1009+14G>A
XM_006710597.2:c.958+14G>A	XP_006710660.1:n.958+14G>A
XM_011541317.1:c.1009+14G>A	XP_011539619.1:n.1009+14G>A
XM_011541318.1:c.1009+14G>A	XP_011539620.1:n.1009+14G>A
XM_011541319.1:c.1009+14G>A	XP_011539621.1:n.1009+14G>A
XM_011541320.1:c.1009+14G>A	XP_011539622.1:n.1009+14G>A
XM_011541321.1:c.1009+14G>A	XP_011539623.1:n.1009+14G>A
XM_011541322.1:c.1009+14G>A	XP_011539624.1:n.1009+14G>A
XM_011541318.2:c.1009+14G>A	XP_011539620.1:n.1009+14G>A
XM_017001120.1:c.1150+14G>A	XP_016856609.1:n.1150+14G>A
XM_017001121.1:c.1099+14G>A	XP_016856610.1:n.1099+14G>A
XM_017001122.1:c.1099+14G>A	XP_016856611.1:n.1099+14G>A
NM_005529.7:c.958+14G>A MANE Select	NP_005520.4:n.958+14G>A
NM_001291860.2:c.958+14G>A	NP_001278789.1:n.958+14G>A