Canonical Allele Identifier: CA1139921402

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21841112C= , CM000663.2:g.21841112C=	GRCh38
NC_000001.10:g.22167605C= , CM000663.1:g.22167605C=	GRCh37
NC_000001.9:g.22040192C=	NCBI36
NG_016740.1:g.101146G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.9502G= MANE Select	ENSP00000363827.3:p.Ala3168=
ENST00000374695.7:c.9502G=	ENSP00000363827.3:p.Ala3168=
NM_001291860.1:c.9505G=	NP_001278789.1:p.Ala3169=
NM_005529.6:c.9502G=	NP_005520.4:p.Ala3168=
XM_006710594.2:c.10048G=	XP_006710657.1:p.Ala3350=
XM_006710595.2:c.10000G=	XP_006710658.1:p.Ala3334=
XM_006710596.2:c.9979G=	XP_006710659.1:p.Ala3327=
XM_006710597.2:c.9502G=	XP_006710660.1:p.Ala3168=
XM_011541317.1:c.10051G=	XP_011539619.1:p.Ala3351=
XM_011541318.1:c.10051G=	XP_011539620.1:p.Ala3351=
XM_011541319.1:c.10051G=	XP_011539621.1:p.Ala3351=
XM_011541320.1:c.9772G=	XP_011539622.1:p.Ala3258=
XM_011541321.1:c.9556G=	XP_011539623.1:p.Ala3186=
XM_011541318.2:c.10051G=	XP_011539620.1:p.Ala3351=
XM_017001120.1:c.9697G=	XP_016856609.1:p.Ala3233=
XM_017001121.1:c.9646G=	XP_016856610.1:p.Ala3216=
XM_017001122.1:c.9643G=	XP_016856611.1:p.Ala3215=
NM_005529.7:c.9502G= MANE Select	NP_005520.4:p.Ala3168=
NM_001291860.2:c.9505G=	NP_001278789.1:p.Ala3169=