Canonical Allele Identifier: CA1955299

Gene: LRP2

Linked Data

• ClinVar Variation Id: 893655
• ClinVar RCV Id: RCV001132324 ; RCV002556847 ; RCV003246714
• dbSNP Id: rs376367082
• ExAC: 2:170115613 C / T
• gnomAD v2: 2-170115613-C-T
• gnomAD v3: 2-169259103-C-T
• gnomAD v4: 2-169259103-C-T
• MyVariant Identifiers: chr2:g.170115613C>T (hg19) ; chr2:g.169259103C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259103C>T , CM000664.2:g.169259103C>T	GRCh38
NC_000002.11:g.170115613C>T , CM000664.1:g.170115613C>T	GRCh37
NC_000002.10:g.169823859C>T	NCBI36
NG_012634.1:g.108510G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2435G>A MANE Select	ENSP00000496870.1:p.Arg812Lys
ENST00000263816.7:c.2435G>A	ENSP00000263816.3:p.Arg812Lys
ENST00000443831.1:c.2024G>A	ENSP00000409813.1:p.Arg675Lys
NM_004525.2:c.2435G>A	NP_004516.2:p.Arg812Lys
XM_011511183.1:c.2435G>A	XP_011509485.1:p.Arg812Lys
XM_011511184.1:c.146G>A	XP_011509486.1:p.Arg49Lys
XM_011511185.1:c.2435G>A	XP_011509487.1:p.Arg812Lys
NM_004525.3:c.2435G>A MANE Select	NP_004516.2:p.Arg812Lys
XM_011511183.3:c.2435G>A	XP_011509485.1:p.Arg812Lys
XM_011511184.2:c.146G>A	XP_011509486.1:p.Arg49Lys