Canonical Allele Identifier: CA349137030

Gene: LRP2

Linked Data

• dbSNP Id: rs2105358831
• MyVariant Identifiers: chr2:g.170010991C>T (hg19) ; chr2:g.169154481C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154481C>T , CM000664.2:g.169154481C>T	GRCh38
NC_000002.11:g.170010991C>T , CM000664.1:g.170010991C>T	GRCh37
NC_000002.10:g.169719237C>T	NCBI36
NG_012634.1:g.213132G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12274G>A MANE Select	ENSP00000496870.1:p.Asp4092Asn
ENST00000649153.1:c.3174G>A
ENST00000650252.1:c.1302G>A	ENSP00000496887.1:p.Gly434=
ENST00000263816.7:c.12274G>A	ENSP00000263816.3:p.Asp4092Asn
NM_004525.2:c.12274G>A	NP_004516.2:p.Asp4092Asn
XM_011511183.1:c.12145G>A	XP_011509485.1:p.Asp4049Asn
XM_011511184.1:c.9985G>A	XP_011509486.1:p.Asp3329Asn
NM_004525.3:c.12274G>A MANE Select	NP_004516.2:p.Asp4092Asn
XM_011511183.3:c.12145G>A	XP_011509485.1:p.Asp4049Asn
XM_011511184.2:c.9985G>A	XP_011509486.1:p.Asp3329Asn