Canonical Allele Identifier: CA1306305783

Gene: LRP2

Linked Data

• dbSNP Id: rs1558982761
• gnomAD v4: 2-169154629-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154629A>T , CM000664.2:g.169154629A>T	GRCh38
NC_000002.11:g.170011139A>T , CM000664.1:g.170011139A>T	GRCh37
NC_000002.10:g.169719385A>T	NCBI36
NG_012634.1:g.212984T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12152-26T>A MANE Select	ENSP00000496870.1:n.12152-26T>A
ENST00000649153.1:c.3052-26T>A
ENST00000650252.1:c.1184-30T>A	ENSP00000496887.1:n.1184-30T>A
ENST00000263816.7:c.12152-26T>A	ENSP00000263816.3:n.12152-26T>A
NM_004525.2:c.12152-26T>A	NP_004516.2:n.12152-26T>A
XM_011511183.1:c.12023-26T>A	XP_011509485.1:n.12023-26T>A
XM_011511184.1:c.9863-26T>A	XP_011509486.1:n.9863-26T>A
NM_004525.3:c.12152-26T>A MANE Select	NP_004516.2:n.12152-26T>A
XM_011511183.3:c.12023-26T>A	XP_011509485.1:n.12023-26T>A
XM_011511184.2:c.9863-26T>A	XP_011509486.1:n.9863-26T>A