Canonical Allele Identifier: CA349149480

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.169985581T>G (hg19) ; chr2:g.169129071T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169129071T>G , CM000664.2:g.169129071T>G	GRCh38
NC_000002.11:g.169985581T>G , CM000664.1:g.169985581T>G	GRCh37
NC_000002.10:g.169693827T>G	NCBI36
NG_012634.1:g.238542A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13742A>C MANE Select	ENSP00000496870.1:p.Asn4581Thr
ENST00000649153.1:c.4551A>C
ENST00000650252.1:c.2733A>C	ENSP00000496887.1:n.2733A>C
ENST00000263816.7:c.13742A>C	ENSP00000263816.3:p.Asn4581Thr
NM_004525.2:c.13742A>C	NP_004516.2:p.Asn4581Thr
XM_011511183.1:c.13613A>C	XP_011509485.1:p.Asn4538Thr
XM_011511184.1:c.11453A>C	XP_011509486.1:p.Asn3818Thr
NM_004525.3:c.13742A>C MANE Select	NP_004516.2:p.Asn4581Thr
XM_011511183.3:c.13613A>C	XP_011509485.1:p.Asn4538Thr
XM_011511184.2:c.11453A>C	XP_011509486.1:p.Asn3818Thr