Canonical Allele Identifier: CA669888

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21832496G>A , CM000663.2:g.21832496G>A	GRCh38
NC_000001.10:g.22158989G>A , CM000663.1:g.22158989G>A	GRCh37
NC_000001.9:g.22031576G>A	NCBI36
NG_016740.1:g.109762C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.11206C>T MANE Select	ENSP00000363827.3:p.Arg3736Trp
ENST00000374695.7:c.11206C>T	ENSP00000363827.3:p.Arg3736Trp
ENST00000635682.1:c.357C>T
NM_001291860.1:c.11209C>T	NP_001278789.1:p.Arg3737Trp
NM_005529.6:c.11206C>T	NP_005520.4:p.Arg3736Trp
XM_006710594.2:c.11770C>T	XP_006710657.1:p.Arg3924Trp
XM_006710595.2:c.11722C>T	XP_006710658.1:p.Arg3908Trp
XM_006710596.2:c.11701C>T	XP_006710659.1:p.Arg3901Trp
XM_006710597.2:c.11224C>T	XP_006710660.1:p.Arg3742Trp
XM_011541317.1:c.11773C>T	XP_011539619.1:p.Arg3925Trp
XM_011541318.1:c.11755C>T	XP_011539620.1:p.Arg3919Trp
XM_011541319.1:c.11773C>T	XP_011539621.1:p.Arg3925Trp
XM_011541320.1:c.11494C>T	XP_011539622.1:p.Arg3832Trp
XM_011541321.1:c.11278C>T	XP_011539623.1:p.Arg3760Trp
XM_011541318.2:c.11755C>T	XP_011539620.1:p.Arg3919Trp
XM_017001120.1:c.11401C>T	XP_016856609.1:p.Arg3801Trp
XM_017001121.1:c.11350C>T	XP_016856610.1:p.Arg3784Trp
XM_017001122.1:c.11347C>T	XP_016856611.1:p.Arg3783Trp
NM_005529.7:c.11206C>T MANE Select	NP_005520.4:p.Arg3736Trp
NM_001291860.2:c.11209C>T	NP_001278789.1:p.Arg3737Trp