Canonical Allele Identifier: CA3072846922

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21847940T= , CM000663.2:g.21847940T=	GRCh38
NC_000001.10:g.22174433T= , CM000663.1:g.22174433T=	GRCh37
NC_000001.9:g.22047020T=	NCBI36
NG_016740.1:g.94318A=

Transcript Alleles

HGVS	Amino-acid Change
NM_005529.7:c.7873+18A= MANE Select	NP_005520.4:n.7873+18A=
ENST00000374695.8:c.7873+18A= MANE Select	ENSP00000363827.3:n.7873+18A=
NM_001291860.1:c.7876+18A=	NP_001278789.1:n.7876+18A=
NM_001291860.2:c.7876+18A=	NP_001278789.1:n.7876+18A=
NM_005529.6:c.7873+18A=	NP_005520.4:n.7873+18A=
ENST00000374695.7:c.7873+18A=	ENSP00000363827.3:n.7873+18A=
ENST00000453796.1:n.19A=
XM_006710594.2:c.8419+18A=	XP_006710657.1:n.8419+18A=
XM_006710595.2:c.8371+18A=	XP_006710658.1:n.8371+18A=
XM_006710596.2:c.8350+18A=	XP_006710659.1:n.8350+18A=
XM_006710597.2:c.7873+18A=	XP_006710660.1:n.7873+18A=
XM_011541317.1:c.8422+18A=	XP_011539619.1:n.8422+18A=
XM_011541318.1:c.8422+18A=	XP_011539620.1:n.8422+18A=
XM_011541318.2:c.8422+18A=	XP_011539620.1:n.8422+18A=
XM_011541319.1:c.8422+18A=	XP_011539621.1:n.8422+18A=
XM_011541320.1:c.8143+18A=	XP_011539622.1:n.8143+18A=
XM_011541321.1:c.7927+18A=	XP_011539623.1:n.7927+18A=
XM_017001120.1:c.8068+18A=	XP_016856609.1:n.8068+18A=
XM_017001121.1:c.8017+18A=	XP_016856610.1:n.8017+18A=
XM_017001122.1:c.8014+18A=	XP_016856611.1:n.8014+18A=