Canonical Allele Identifier: CA1158130878
Gene: HSPG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21834266A= , CM000663.2:g.21834266A= GRCh38
NC_000001.10:g.22160759A= , CM000663.1:g.22160759A= GRCh37
NC_000001.9:g.22033346A= NCBI36
NG_016740.1:g.107992T=

Transcript Alleles

HGVS Amino-acid change
ENST00000374695.8:c.10721-341T= MANE Select ENSP00000363827.3:n.10721-341T=
ENST00000374695.7:c.10721-341T= ENSP00000363827.3:n.10721-341T=
ENST00000471322.2:n.1076-341T=
NM_001291860.1:c.10724-341T= NP_001278789.1:n.10724-341T=
NM_005529.6:c.10721-341T= NP_005520.4:n.10721-341T=
XM_006710594.2:c.11267-341T= XP_006710657.1:n.11267-341T=
XM_006710595.2:c.11219-341T= XP_006710658.1:n.11219-341T=
XM_006710596.2:c.11198-341T= XP_006710659.1:n.11198-341T=
XM_006710597.2:c.10721-341T= XP_006710660.1:n.10721-341T=
XM_011541317.1:c.11270-341T= XP_011539619.1:n.11270-341T=
XM_011541318.1:c.11270-341T= XP_011539620.1:n.11270-341T=
XM_011541319.1:c.11270-341T= XP_011539621.1:n.11270-341T=
XM_011541320.1:c.10991-341T= XP_011539622.1:n.10991-341T=
XM_011541321.1:c.10775-341T= XP_011539623.1:n.10775-341T=
XM_011541318.2:c.11270-341T= XP_011539620.1:n.11270-341T=
XM_017001120.1:c.10916-341T= XP_016856609.1:n.10916-341T=
XM_017001121.1:c.10865-341T= XP_016856610.1:n.10865-341T=
XM_017001122.1:c.10862-341T= XP_016856611.1:n.10862-341T=
NM_005529.7:c.10721-341T= MANE Select NP_005520.4:n.10721-341T=
NM_001291860.2:c.10724-341T= NP_001278789.1:n.10724-341T=