Canonical Allele Identifier: CA760480383

Gene: LRP2

Linked Data

• dbSNP Id: rs1311317274
• gnomAD v3: 2-169259337-G-GA
• gnomAD v4: 2-169259337-G-GA
• MyVariant Identifiers: chr2:g.170115847_170115848insA (hg19) ; chr2:g.169259337_169259338insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259339dup , CM000664.2:g.169259339dup	GRCh38
NC_000002.11:g.170115849dup , CM000664.1:g.170115849dup	GRCh37
NC_000002.10:g.169824095dup	NCBI36
NG_012634.1:g.108275dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2321-121dup MANE Select	ENSP00000496870.1:n.2321-121dup
ENST00000263816.7:c.2321-121dup	ENSP00000263816.3:n.2321-121dup
ENST00000443831.1:c.1910-121dup	ENSP00000409813.1:n.1910-121dup
NM_004525.2:c.2321-121dup	NP_004516.2:n.2321-121dup
XM_011511183.1:c.2321-121dup	XP_011509485.1:n.2321-121dup
XM_011511184.1:c.32-121dup	XP_011509486.1:n.32-121dup
XM_011511185.1:c.2321-121dup	XP_011509487.1:n.2321-121dup
NM_004525.3:c.2321-121dup MANE Select	NP_004516.2:n.2321-121dup
XM_011511183.3:c.2321-121dup	XP_011509485.1:n.2321-121dup
XM_011511184.2:c.32-121dup	XP_011509486.1:n.32-121dup