Canonical Allele Identifier: CA1139990392

Gene: LDLRAD2 HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21823627C= , CM000663.2:g.21823627C=	GRCh38
NC_000001.10:g.22150120C= , CM000663.1:g.22150120C=	GRCh37
NC_000001.9:g.22022707C=	NCBI36
NG_016740.1:g.118631G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344642.7:c.*1412C= (LDLRAD2) MANE Select	ENSP00000340988.2:n.*1412C=
ENST00000374695.8:c.12992G= (HSPG2) MANE Select	ENSP00000363827.3:p.Ser4331=
ENST00000344642.6:c.*1412C= (LDLRAD2)	ENSP00000340988.2:n.*1412C=
ENST00000374695.7:c.12992G= (HSPG2)	ENSP00000363827.3:p.Ser4331=
ENST00000481644.1:n.640G= (HSPG2)
ENST00000486901.1:n.2331G= (HSPG2)
ENST00000543870.1:c.*219-283C= (LDLRAD2)	ENSP00000444097.1:n.*219-283C=
NM_001013693.2:c.*1412C= (LDLRAD2)	NP_001013715.2:n.*1412C=
NM_001291860.1:c.12995G= (HSPG2)	NP_001278789.1:p.Ser4332=
NM_005529.6:c.12992G= (HSPG2)	NP_005520.4:p.Ser4331=
XM_006710594.2:c.13556G= (HSPG2)	XP_006710657.1:p.Ser4519=
XM_006710595.2:c.13508G= (HSPG2)	XP_006710658.1:p.Ser4503=
XM_006710596.2:c.13487G= (HSPG2)	XP_006710659.1:p.Ser4496=
XM_006710597.2:c.13010G= (HSPG2)	XP_006710660.1:p.Ser4337=
XM_011541317.1:c.13559G= (HSPG2)	XP_011539619.1:p.Ser4520=
XM_011541318.1:c.13541G= (HSPG2)	XP_011539620.1:p.Ser4514=
XM_011541319.1:c.13436G= (HSPG2)	XP_011539621.1:p.Ser4479=
XM_011541320.1:c.13280G= (HSPG2)	XP_011539622.1:p.Ser4427=
XM_011541321.1:c.13064G= (HSPG2)	XP_011539623.1:p.Ser4355=
XM_011541318.2:c.13541G= (HSPG2)	XP_011539620.1:p.Ser4514=
XM_017001120.1:c.13187G= (HSPG2)	XP_016856609.1:p.Ser4396=
XM_017001121.1:c.13136G= (HSPG2)	XP_016856610.1:p.Ser4379=
XM_017001122.1:c.13133G= (HSPG2)	XP_016856611.1:p.Ser4378=
NM_005529.7:c.12992G= (HSPG2) MANE Select	NP_005520.4:p.Ser4331=
NM_001013693.3:c.*1412C= (LDLRAD2) MANE Select	NP_001013715.2:n.*1412C=
NM_001291860.2:c.12995G= (HSPG2)	NP_001278789.1:p.Ser4332=