Canonical Allele Identifier: CA1306353986

Gene: LRP2

Linked Data

• dbSNP Id: rs1690456896

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259576_169259581dup , CM000664.2:g.169259576_169259581dup	GRCh38
NC_000002.11:g.170116086_170116091dup , CM000664.1:g.170116086_170116091dup	GRCh37
NC_000002.10:g.169824332_169824337dup	NCBI36
NG_012634.1:g.108035_108040dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2321-361_2321-356dup MANE Select	ENSP00000496870.1:n.2321-361_2321-356dup
ENST00000263816.7:c.2321-361_2321-356dup	ENSP00000263816.3:n.2321-361_2321-356dup
ENST00000443831.1:c.1910-361_1910-356dup	ENSP00000409813.1:n.1910-361_1910-356dup
NM_004525.2:c.2321-361_2321-356dup	NP_004516.2:n.2321-361_2321-356dup
XM_011511183.1:c.2321-361_2321-356dup	XP_011509485.1:n.2321-361_2321-356dup
XM_011511184.1:c.32-361_32-356dup	XP_011509486.1:n.32-361_32-356dup
XM_011511185.1:c.2321-361_2321-356dup	XP_011509487.1:n.2321-361_2321-356dup
NM_004525.3:c.2321-361_2321-356dup MANE Select	NP_004516.2:n.2321-361_2321-356dup
XM_011511183.3:c.2321-361_2321-356dup	XP_011509485.1:n.2321-361_2321-356dup
XM_011511184.2:c.32-361_32-356dup	XP_011509486.1:n.32-361_32-356dup