Canonical Allele Identifier: CA2661823093

Gene: LRP2

Linked Data

• gnomAD v4: 2-169259345-TAAAAAAAAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259357_169259366del , CM000664.2:g.169259357_169259366del	GRCh38
NC_000002.11:g.170115867_170115876del , CM000664.1:g.170115867_170115876del	GRCh37
NC_000002.10:g.169824113_169824122del	NCBI36
NG_012634.1:g.108258_108267del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2321-138_2321-129del MANE Select	ENSP00000496870.1:n.2321-138_2321-129del
ENST00000263816.7:c.2321-138_2321-129del	ENSP00000263816.3:n.2321-138_2321-129del
ENST00000443831.1:c.1910-138_1910-129del	ENSP00000409813.1:n.1910-138_1910-129del
NM_004525.2:c.2321-138_2321-129del	NP_004516.2:n.2321-138_2321-129del
XM_011511183.1:c.2321-138_2321-129del	XP_011509485.1:n.2321-138_2321-129del
XM_011511184.1:c.32-138_32-129del	XP_011509486.1:n.32-138_32-129del
XM_011511185.1:c.2321-138_2321-129del	XP_011509487.1:n.2321-138_2321-129del
NM_004525.3:c.2321-138_2321-129del MANE Select	NP_004516.2:n.2321-138_2321-129del
XM_011511183.3:c.2321-138_2321-129del	XP_011509485.1:n.2321-138_2321-129del
XM_011511184.2:c.32-138_32-129del	XP_011509486.1:n.32-138_32-129del