Canonical Allele Identifier: CA1158157620

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21899279G= , CM000663.2:g.21899279G=	GRCh38
NC_000001.10:g.22225772G= , CM000663.1:g.22225772G=	GRCh37
NC_000001.9:g.22098359G=	NCBI36
NG_016740.1:g.42979C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000374695.8:c.64-2969C= MANE Select	ENSP00000363827.3:n.64-2969C=
ENST00000374695.7:c.64-2969C=	ENSP00000363827.3:n.64-2969C=
NM_001291860.1:c.64-2969C=	NP_001278789.1:n.64-2969C=
NM_005529.6:c.64-2969C=	NP_005520.4:n.64-2969C=
XM_006710594.2:c.64-2969C=	XP_006710657.1:n.64-2969C=
XM_006710595.2:c.64-2969C=	XP_006710658.1:n.64-2969C=
XM_006710596.2:c.64-2969C=	XP_006710659.1:n.64-2969C=
XM_006710597.2:c.64-2969C=	XP_006710660.1:n.64-2969C=
XM_011541317.1:c.64-2969C=	XP_011539619.1:n.64-2969C=
XM_011541318.1:c.64-2969C=	XP_011539620.1:n.64-2969C=
XM_011541319.1:c.64-2969C=	XP_011539621.1:n.64-2969C=
XM_011541320.1:c.64-2969C=	XP_011539622.1:n.64-2969C=
XM_011541321.1:c.64-2969C=	XP_011539623.1:n.64-2969C=
XM_011541322.1:c.64-2969C=	XP_011539624.1:n.64-2969C=
XM_011541318.2:c.64-2969C=	XP_011539620.1:n.64-2969C=
NM_005529.7:c.64-2969C= MANE Select	NP_005520.4:n.64-2969C=
NM_001291860.2:c.64-2969C=	NP_001278789.1:n.64-2969C=