Canonical Allele Identifier: CA1139921407

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21842352A= , CM000663.2:g.21842352A=	GRCh38
NC_000001.10:g.22168845A= , CM000663.1:g.22168845A=	GRCh37
NC_000001.9:g.22041432A=	NCBI36
NG_016740.1:g.99906T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.8939T= MANE Select	ENSP00000363827.3:p.Leu2980=
ENST00000374695.7:c.8939T=	ENSP00000363827.3:p.Leu2980=
NM_001291860.1:c.8942T=	NP_001278789.1:p.Leu2981=
NM_005529.6:c.8939T=	NP_005520.4:p.Leu2980=
XM_006710594.2:c.9485T=	XP_006710657.1:p.Leu3162=
XM_006710595.2:c.9437T=	XP_006710658.1:p.Leu3146=
XM_006710596.2:c.9416T=	XP_006710659.1:p.Leu3139=
XM_006710597.2:c.8939T=	XP_006710660.1:p.Leu2980=
XM_011541317.1:c.9488T=	XP_011539619.1:p.Leu3163=
XM_011541318.1:c.9488T=	XP_011539620.1:p.Leu3163=
XM_011541319.1:c.9488T=	XP_011539621.1:p.Leu3163=
XM_011541320.1:c.9209T=	XP_011539622.1:p.Leu3070=
XM_011541321.1:c.8993T=	XP_011539623.1:p.Leu2998=
XM_011541318.2:c.9488T=	XP_011539620.1:p.Leu3163=
XM_017001120.1:c.9134T=	XP_016856609.1:p.Leu3045=
XM_017001121.1:c.9083T=	XP_016856610.1:p.Leu3028=
XM_017001122.1:c.9080T=	XP_016856611.1:p.Leu3027=
NM_005529.7:c.8939T= MANE Select	NP_005520.4:p.Leu2980=
NM_001291860.2:c.8942T=	NP_001278789.1:p.Leu2981=