Canonical Allele Identifier: CA670281

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21839092G>T , CM000663.2:g.21839092G>T	GRCh38
NC_000001.10:g.22165585G>T , CM000663.1:g.22165585G>T	GRCh37
NC_000001.9:g.22038172G>T	NCBI36
NG_016740.1:g.103166C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005529.7:c.9890-7C>A MANE Select	NP_005520.4:n.9890-7C>A
ENST00000374695.8:c.9890-7C>A MANE Select	ENSP00000363827.3:n.9890-7C>A
NM_001291860.1:c.9893-7C>A	NP_001278789.1:n.9893-7C>A
NM_001291860.2:c.9893-7C>A	NP_001278789.1:n.9893-7C>A
NM_005529.6:c.9890-7C>A	NP_005520.4:n.9890-7C>A
ENST00000374695.7:c.9890-7C>A	ENSP00000363827.3:n.9890-7C>A
XM_006710594.2:c.10436-7C>A	XP_006710657.1:n.10436-7C>A
XM_006710595.2:c.10388-7C>A	XP_006710658.1:n.10388-7C>A
XM_006710596.2:c.10367-7C>A	XP_006710659.1:n.10367-7C>A
XM_006710597.2:c.9890-7C>A	XP_006710660.1:n.9890-7C>A
XM_011541317.1:c.10439-7C>A	XP_011539619.1:n.10439-7C>A
XM_011541318.1:c.10439-7C>A	XP_011539620.1:n.10439-7C>A
XM_011541318.2:c.10439-7C>A	XP_011539620.1:n.10439-7C>A
XM_011541319.1:c.10439-7C>A	XP_011539621.1:n.10439-7C>A
XM_011541320.1:c.10160-7C>A	XP_011539622.1:n.10160-7C>A
XM_011541321.1:c.9944-7C>A	XP_011539623.1:n.9944-7C>A
XM_017001120.1:c.10085-7C>A	XP_016856609.1:n.10085-7C>A
XM_017001121.1:c.10034-7C>A	XP_016856610.1:n.10034-7C>A
XM_017001122.1:c.10031-7C>A	XP_016856611.1:n.10031-7C>A