Canonical Allele Identifier: CA349157973

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170115541A>G (hg19) ; chr2:g.169259031A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169259031A>G , CM000664.2:g.169259031A>G	GRCh38
NC_000002.11:g.170115541A>G , CM000664.1:g.170115541A>G	GRCh37
NC_000002.10:g.169823787A>G	NCBI36
NG_012634.1:g.108582T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2507T>C MANE Select	ENSP00000496870.1:p.Phe836Ser
ENST00000263816.7:c.2507T>C	ENSP00000263816.3:p.Phe836Ser
ENST00000443831.1:c.2096T>C	ENSP00000409813.1:p.Phe699Ser
NM_004525.2:c.2507T>C	NP_004516.2:p.Phe836Ser
XM_011511183.1:c.2507T>C	XP_011509485.1:p.Phe836Ser
XM_011511184.1:c.218T>C	XP_011509486.1:p.Phe73Ser
XM_011511185.1:c.2507T>C	XP_011509487.1:p.Phe836Ser
NM_004525.3:c.2507T>C MANE Select	NP_004516.2:p.Phe836Ser
XM_011511183.3:c.2507T>C	XP_011509485.1:p.Phe836Ser
XM_011511184.2:c.218T>C	XP_011509486.1:p.Phe73Ser