Canonical Allele Identifier: CA2838196870

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21842003del , CM000663.2:g.21842003del	GRCh38
NC_000001.10:g.22168496del , CM000663.1:g.22168496del	GRCh37
NC_000001.9:g.22041083del	NCBI36
NG_016740.1:g.100257del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.9193+1del
ENST00000374695.7:c.9193+1del
NM_001291860.1:c.9196+1del
NM_005529.6:c.9193+1del
XM_006710594.2:c.9739+1del
XM_006710595.2:c.9691+1del
XM_006710596.2:c.9670+1del
XM_006710597.2:c.9193+1del
XM_011541317.1:c.9742+1del
XM_011541318.1:c.9742+1del
XM_011541319.1:c.9742+1del
XM_011541320.1:c.9463+1del
XM_011541321.1:c.9247+1del
XM_011541318.2:c.9742+1del
XM_017001120.1:c.9388+1del
XM_017001121.1:c.9337+1del
XM_017001122.1:c.9334+1del
NM_005529.7:c.9193+1del
NM_001291860.2:c.9196+1del