Canonical Allele Identifier: CA1158130882
Gene: HSPG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21834270_21834272delinsATT , CM000663.2:g.21834270_21834272delinsATT GRCh38
NC_000001.10:g.22160763_22160765delinsATT , CM000663.1:g.22160763_22160765delinsATT GRCh37
NC_000001.9:g.22033350_22033352delinsATT NCBI36
NG_016740.1:g.107986_107988delinsAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000374695.8:c.10721-347_10721-345delinsAAT MANE Select ENSP00000363827.3:n.10721-347_10721-345delinsAAT
ENST00000374695.7:c.10721-347_10721-345delinsAAT ENSP00000363827.3:n.10721-347_10721-345delinsAAT
ENST00000471322.2:n.1076-347_1076-345delinsAAT
NM_001291860.1:c.10724-347_10724-345delinsAAT NP_001278789.1:n.10724-347_10724-345delinsAAT
NM_005529.6:c.10721-347_10721-345delinsAAT NP_005520.4:n.10721-347_10721-345delinsAAT
XM_006710594.2:c.11267-347_11267-345delinsAAT XP_006710657.1:n.11267-347_11267-345delinsAAT
XM_006710595.2:c.11219-347_11219-345delinsAAT XP_006710658.1:n.11219-347_11219-345delinsAAT
XM_006710596.2:c.11198-347_11198-345delinsAAT XP_006710659.1:n.11198-347_11198-345delinsAAT
XM_006710597.2:c.10721-347_10721-345delinsAAT XP_006710660.1:n.10721-347_10721-345delinsAAT
XM_011541317.1:c.11270-347_11270-345delinsAAT XP_011539619.1:n.11270-347_11270-345delinsAAT
XM_011541318.1:c.11270-347_11270-345delinsAAT XP_011539620.1:n.11270-347_11270-345delinsAAT
XM_011541319.1:c.11270-347_11270-345delinsAAT XP_011539621.1:n.11270-347_11270-345delinsAAT
XM_011541320.1:c.10991-347_10991-345delinsAAT XP_011539622.1:n.10991-347_10991-345delinsAAT
XM_011541321.1:c.10775-347_10775-345delinsAAT XP_011539623.1:n.10775-347_10775-345delinsAAT
XM_011541318.2:c.11270-347_11270-345delinsAAT XP_011539620.1:n.11270-347_11270-345delinsAAT
XM_017001120.1:c.10916-347_10916-345delinsAAT XP_016856609.1:n.10916-347_10916-345delinsAAT
XM_017001121.1:c.10865-347_10865-345delinsAAT XP_016856610.1:n.10865-347_10865-345delinsAAT
XM_017001122.1:c.10862-347_10862-345delinsAAT XP_016856611.1:n.10862-347_10862-345delinsAAT
NM_005529.7:c.10721-347_10721-345delinsAAT MANE Select NP_005520.4:n.10721-347_10721-345delinsAAT
NM_001291860.2:c.10724-347_10724-345delinsAAT NP_001278789.1:n.10724-347_10724-345delinsAAT