Canonical Allele Identifier: CA429921141

Gene: LRP2

Linked Data

• dbSNP Id: rs1690433649
• MyVariant Identifiers: chr2:g.170115675A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259165A>G , CM000664.2:g.169259165A>G	GRCh38
NC_000002.11:g.170115675A>G , CM000664.1:g.170115675A>G	GRCh37
NC_000002.10:g.169823921A>G	NCBI36
NG_012634.1:g.108448T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2373T>C MANE Select	ENSP00000496870.1:p.Phe791=
ENST00000263816.7:c.2373T>C	ENSP00000263816.3:p.Phe791=
ENST00000443831.1:c.1962T>C	ENSP00000409813.1:p.Phe654=
NM_004525.2:c.2373T>C	NP_004516.2:p.Phe791=
XM_011511183.1:c.2373T>C	XP_011509485.1:p.Phe791=
XM_011511184.1:c.84T>C	XP_011509486.1:p.Phe28=
XM_011511185.1:c.2373T>C	XP_011509487.1:p.Phe791=
NM_004525.3:c.2373T>C MANE Select	NP_004516.2:p.Phe791=
XM_011511183.3:c.2373T>C	XP_011509485.1:p.Phe791=
XM_011511184.2:c.84T>C	XP_011509486.1:p.Phe28=