Canonical Allele Identifier: CA349136886

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170010968A>G (hg19) ; chr2:g.169154458A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154458A>G , CM000664.2:g.169154458A>G	GRCh38
NC_000002.11:g.170010968A>G , CM000664.1:g.170010968A>G	GRCh37
NC_000002.10:g.169719214A>G	NCBI36
NG_012634.1:g.213155T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12295+2T>C MANE Select	ENSP00000496870.1:n.12295+2T>C
ENST00000649153.1:c.3195+2T>C
ENST00000650252.1:c.1323+2T>C	ENSP00000496887.1:n.1323+2T>C
ENST00000263816.7:c.12295+2T>C	ENSP00000263816.3:n.12295+2T>C
NM_004525.2:c.12295+2T>C	NP_004516.2:n.12295+2T>C
XM_011511183.1:c.12166+2T>C	XP_011509485.1:n.12166+2T>C
XM_011511184.1:c.10006+2T>C	XP_011509486.1:n.10006+2T>C
NM_004525.3:c.12295+2T>C MANE Select	NP_004516.2:n.12295+2T>C
XM_011511183.3:c.12166+2T>C	XP_011509485.1:n.12166+2T>C
XM_011511184.2:c.10006+2T>C	XP_011509486.1:n.10006+2T>C