Canonical Allele Identifier: CA1158143111

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21864095C= , CM000663.2:g.21864095C=	GRCh38
NC_000001.10:g.22190588C= , CM000663.1:g.22190588C=	GRCh37
NC_000001.9:g.22063175C=	NCBI36
NG_016740.1:g.78163G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.4740+5G= MANE Select	ENSP00000363827.3:n.4740+5G=
ENST00000374695.7:c.4740+5G=	ENSP00000363827.3:n.4740+5G=
NM_001291860.1:c.4743+5G=	NP_001278789.1:n.4743+5G=
NM_005529.6:c.4740+5G=	NP_005520.4:n.4740+5G=
XM_006710594.2:c.5286+5G=	XP_006710657.1:n.5286+5G=
XM_006710595.2:c.5238+5G=	XP_006710658.1:n.5238+5G=
XM_006710596.2:c.5217+5G=	XP_006710659.1:n.5217+5G=
XM_006710597.2:c.4740+5G=	XP_006710660.1:n.4740+5G=
XM_011541317.1:c.5289+5G=	XP_011539619.1:n.5289+5G=
XM_011541318.1:c.5289+5G=	XP_011539620.1:n.5289+5G=
XM_011541319.1:c.5289+5G=	XP_011539621.1:n.5289+5G=
XM_011541320.1:c.5289+5G=	XP_011539622.1:n.5289+5G=
XM_011541321.1:c.4794+5G=	XP_011539623.1:n.4794+5G=
XM_011541322.1:c.5289+5G=	XP_011539624.1:n.5289+5G=
XM_011541318.2:c.5289+5G=	XP_011539620.1:n.5289+5G=
XM_017001120.1:c.4935+5G=	XP_016856609.1:n.4935+5G=
XM_017001121.1:c.4884+5G=	XP_016856610.1:n.4884+5G=
XM_017001122.1:c.4881+5G=	XP_016856611.1:n.4881+5G=
NM_005529.7:c.4740+5G= MANE Select	NP_005520.4:n.4740+5G=
NM_001291860.2:c.4743+5G=	NP_001278789.1:n.4743+5G=