Canonical Allele Identifier: CA916127306

Gene: HSPG2

Linked Data

• dbSNP Id: rs1557682733

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21834282del , CM000663.2:g.21834282del	GRCh38
NC_000001.10:g.22160775del , CM000663.1:g.22160775del	GRCh37
NC_000001.9:g.22033362del	NCBI36
NG_016740.1:g.107976del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.10721-357del MANE Select	ENSP00000363827.3:n.10721-357del
ENST00000374695.7:c.10721-357del	ENSP00000363827.3:n.10721-357del
ENST00000471322.2:n.1076-357del
NM_001291860.1:c.10724-357del	NP_001278789.1:n.10724-357del
NM_005529.6:c.10721-357del	NP_005520.4:n.10721-357del
XM_006710594.2:c.11267-357del	XP_006710657.1:n.11267-357del
XM_006710595.2:c.11219-357del	XP_006710658.1:n.11219-357del
XM_006710596.2:c.11198-357del	XP_006710659.1:n.11198-357del
XM_006710597.2:c.10721-357del	XP_006710660.1:n.10721-357del
XM_011541317.1:c.11270-357del	XP_011539619.1:n.11270-357del
XM_011541318.1:c.11270-357del	XP_011539620.1:n.11270-357del
XM_011541319.1:c.11270-357del	XP_011539621.1:n.11270-357del
XM_011541320.1:c.10991-357del	XP_011539622.1:n.10991-357del
XM_011541321.1:c.10775-357del	XP_011539623.1:n.10775-357del
XM_011541318.2:c.11270-357del	XP_011539620.1:n.11270-357del
XM_017001120.1:c.10916-357del	XP_016856609.1:n.10916-357del
XM_017001121.1:c.10865-357del	XP_016856610.1:n.10865-357del
XM_017001122.1:c.10862-357del	XP_016856611.1:n.10862-357del
NM_005529.7:c.10721-357del MANE Select	NP_005520.4:n.10721-357del
NM_001291860.2:c.10724-357del	NP_001278789.1:n.10724-357del