Canonical Allele Identifier: CA429920361

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170104015A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169247505A>G , CM000664.2:g.169247505A>G	GRCh38
NC_000002.11:g.170104015A>G , CM000664.1:g.170104015A>G	GRCh37
NC_000002.10:g.169812261A>G	NCBI36
NG_012634.1:g.120108T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.2781T>C MANE Select	ENSP00000496870.1:p.Phe927=
ENST00000263816.7:c.2781T>C	ENSP00000263816.3:p.Phe927=
ENST00000443831.1:c.2370T>C	ENSP00000409813.1:p.Phe790=
NM_004525.2:c.2781T>C	NP_004516.2:p.Phe927=
XM_011511183.1:c.2781T>C	XP_011509485.1:p.Phe927=
XM_011511184.1:c.492T>C	XP_011509486.1:p.Phe164=
XM_011511185.1:c.2781T>C	XP_011509487.1:p.Phe927=
NM_004525.3:c.2781T>C MANE Select	NP_004516.2:p.Phe927=
XM_011511183.3:c.2781T>C	XP_011509485.1:p.Phe927=
XM_011511184.2:c.492T>C	XP_011509486.1:p.Phe164=