Canonical Allele Identifier: CA10609142

Gene: LDLRAD2 HSPG2

Linked Data

• ClinVar Variation Id: 295691
• ClinVar RCV Id: RCV000349302 ; RCV000387452
• dbSNP Id: rs777311066
• gnomAD v2: 1-22149706-C-T
• gnomAD v3: 1-21823213-C-T
• gnomAD v4: 1-21823213-C-T
• MyVariant Identifiers: chr1:g.22149706C>T (hg19) ; chr1:g.21823213C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21823213C>T , CM000663.2:g.21823213C>T	GRCh38
NC_000001.10:g.22149706C>T , CM000663.1:g.22149706C>T	GRCh37
NC_000001.9:g.22022293C>T	NCBI36
NG_016740.1:g.119045G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344642.7:c.*998C>T (LDLRAD2) MANE Select	ENSP00000340988.2:n.*998C>T
ENST00000374695.8:c.*103G>A (HSPG2) MANE Select	ENSP00000363827.3:n.*103G>A
ENST00000344642.6:c.*998C>T (LDLRAD2)	ENSP00000340988.2:n.*998C>T
ENST00000374695.7:c.*103G>A (HSPG2)	ENSP00000363827.3:n.*103G>A
ENST00000486901.1:n.2618G>A (HSPG2)
ENST00000543870.1:c.*219-697C>T (LDLRAD2)	ENSP00000444097.1:n.*219-697C>T
NM_001013693.2:c.*998C>T (LDLRAD2)	NP_001013715.2:n.*998C>T
NM_001291860.1:c.*103G>A (HSPG2)	NP_001278789.1:n.*103G>A
NM_005529.6:c.*103G>A (HSPG2)	NP_005520.4:n.*103G>A
XM_005245873.3:c.*1546C>T (LDLRAD2)	XP_005245930.1:n.*1546C>T
XM_006710594.2:c.*103G>A (HSPG2)	XP_006710657.1:n.*103G>A
XM_006710595.2:c.*103G>A (HSPG2)	XP_006710658.1:n.*103G>A
XM_006710596.2:c.*103G>A (HSPG2)	XP_006710659.1:n.*103G>A
XM_006710597.2:c.*103G>A (HSPG2)	XP_006710660.1:n.*103G>A
XM_011541317.1:c.*103G>A (HSPG2)	XP_011539619.1:n.*103G>A
XM_011541318.1:c.*103G>A (HSPG2)	XP_011539620.1:n.*103G>A
XM_011541319.1:c.*103G>A (HSPG2)	XP_011539621.1:n.*103G>A
XM_011541320.1:c.*103G>A (HSPG2)	XP_011539622.1:n.*103G>A
XM_011541321.1:c.*103G>A (HSPG2)	XP_011539623.1:n.*103G>A
XM_011541318.2:c.*103G>A (HSPG2)	XP_011539620.1:n.*103G>A
XM_017001120.1:c.*103G>A (HSPG2)	XP_016856609.1:n.*103G>A
XM_017001121.1:c.*103G>A (HSPG2)	XP_016856610.1:n.*103G>A
XM_017001122.1:c.*103G>A (HSPG2)	XP_016856611.1:n.*103G>A
NM_005529.7:c.*103G>A (HSPG2) MANE Select	NP_005520.4:n.*103G>A
NM_001013693.3:c.*998C>T (LDLRAD2) MANE Select	NP_001013715.2:n.*998C>T
NM_001291860.2:c.*103G>A (HSPG2)	NP_001278789.1:n.*103G>A