Canonical Allele Identifier: CA1139838952

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21864961G= , CM000663.2:g.21864961G=	GRCh38
NC_000001.10:g.22191454G= , CM000663.1:g.22191454G=	GRCh37
NC_000001.9:g.22064041G=	NCBI36
NG_016740.1:g.77297C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.4508C= MANE Select	ENSP00000363827.3:p.Ala1503=
ENST00000374695.7:c.4508C=	ENSP00000363827.3:p.Ala1503=
NM_001291860.1:c.4511C=	NP_001278789.1:p.Ala1504=
NM_005529.6:c.4508C=	NP_005520.4:p.Ala1503=
XM_006710594.2:c.5054C=	XP_006710657.1:p.Ala1685=
XM_006710595.2:c.5006C=	XP_006710658.1:p.Ala1669=
XM_006710596.2:c.4985C=	XP_006710659.1:p.Ala1662=
XM_006710597.2:c.4508C=	XP_006710660.1:p.Ala1503=
XM_011541317.1:c.5057C=	XP_011539619.1:p.Ala1686=
XM_011541318.1:c.5057C=	XP_011539620.1:p.Ala1686=
XM_011541319.1:c.5057C=	XP_011539621.1:p.Ala1686=
XM_011541320.1:c.5057C=	XP_011539622.1:p.Ala1686=
XM_011541321.1:c.4562C=	XP_011539623.1:p.Ala1521=
XM_011541322.1:c.5057C=	XP_011539624.1:p.Ala1686=
XM_011541318.2:c.5057C=	XP_011539620.1:p.Ala1686=
XM_017001120.1:c.4703C=	XP_016856609.1:p.Ala1568=
XM_017001121.1:c.4652C=	XP_016856610.1:p.Ala1551=
XM_017001122.1:c.4649C=	XP_016856611.1:p.Ala1550=
NM_005529.7:c.4508C= MANE Select	NP_005520.4:p.Ala1503=
NM_001291860.2:c.4511C=	NP_001278789.1:p.Ala1504=