Canonical Allele Identifier: CA669982

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21833528G>A , CM000663.2:g.21833528G>A	GRCh38
NC_000001.10:g.22160021G>A , CM000663.1:g.22160021G>A	GRCh37
NC_000001.9:g.22032608G>A	NCBI36
NG_016740.1:g.108730C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.10917C>T MANE Select	ENSP00000363827.3:p.Tyr3639=
ENST00000374695.7:c.10917C>T	ENSP00000363827.3:p.Tyr3639=
ENST00000471322.2:n.1272C>T
ENST00000635682.1:c.50C>T
NM_001291860.1:c.10920C>T	NP_001278789.1:p.Tyr3640=
NM_005529.6:c.10917C>T	NP_005520.4:p.Tyr3639=
XM_006710594.2:c.11463C>T	XP_006710657.1:p.Tyr3821=
XM_006710595.2:c.11415C>T	XP_006710658.1:p.Tyr3805=
XM_006710596.2:c.11394C>T	XP_006710659.1:p.Tyr3798=
XM_006710597.2:c.10917C>T	XP_006710660.1:p.Tyr3639=
XM_011541317.1:c.11466C>T	XP_011539619.1:p.Tyr3822=
XM_011541318.1:c.11466C>T	XP_011539620.1:p.Tyr3822=
XM_011541319.1:c.11466C>T	XP_011539621.1:p.Tyr3822=
XM_011541320.1:c.11187C>T	XP_011539622.1:p.Tyr3729=
XM_011541321.1:c.10971C>T	XP_011539623.1:p.Tyr3657=
XM_011541318.2:c.11466C>T	XP_011539620.1:p.Tyr3822=
XM_017001120.1:c.11112C>T	XP_016856609.1:p.Tyr3704=
XM_017001121.1:c.11061C>T	XP_016856610.1:p.Tyr3687=
XM_017001122.1:c.11058C>T	XP_016856611.1:p.Tyr3686=
NM_005529.7:c.10917C>T MANE Select	NP_005520.4:p.Tyr3639=
NM_001291860.2:c.10920C>T	NP_001278789.1:p.Tyr3640=