Canonical Allele Identifier: CA429922593

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170011061A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154551A>G , CM000664.2:g.169154551A>G	GRCh38
NC_000002.11:g.170011061A>G , CM000664.1:g.170011061A>G	GRCh37
NC_000002.10:g.169719307A>G	NCBI36
NG_012634.1:g.213062T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12204T>C MANE Select	ENSP00000496870.1:p.Asn4068=
ENST00000649153.1:c.3104T>C
ENST00000650252.1:c.1232T>C	ENSP00000496887.1:p.Ile411Thr
ENST00000263816.7:c.12204T>C	ENSP00000263816.3:p.Asn4068=
NM_004525.2:c.12204T>C	NP_004516.2:p.Asn4068=
XM_011511183.1:c.12075T>C	XP_011509485.1:p.Asn4025=
XM_011511184.1:c.9915T>C	XP_011509486.1:p.Asn3305=
NM_004525.3:c.12204T>C MANE Select	NP_004516.2:p.Asn4068=
XM_011511183.3:c.12075T>C	XP_011509485.1:p.Asn4025=
XM_011511184.2:c.9915T>C	XP_011509486.1:p.Asn3305=