Canonical Allele Identifier: CA1952967

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169162611A>C , CM000664.2:g.169162611A>C	GRCh38
NC_000002.11:g.170019121A>C , CM000664.1:g.170019121A>C	GRCh37
NC_000002.10:g.169727367A>C	NCBI36
NG_012634.1:g.205002T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004525.3:c.11759-11T>G MANE Select	NP_004516.2:n.11759-11T>G
ENST00000649046.1:c.11759-11T>G MANE Select	ENSP00000496870.1:n.11759-11T>G
NM_004525.2:c.11759-11T>G	NP_004516.2:n.11759-11T>G
ENST00000263816.7:c.11759-11T>G	ENSP00000263816.3:n.11759-11T>G
ENST00000649153.1:c.2659-11T>G
ENST00000650252.1:c.791-11T>G	ENSP00000496887.1:n.791-11T>G
XM_011511183.1:c.11630-11T>G	XP_011509485.1:n.11630-11T>G
XM_011511183.3:c.11630-11T>G	XP_011509485.1:n.11630-11T>G
XM_011511184.1:c.9470-11T>G	XP_011509486.1:n.9470-11T>G
XM_011511184.2:c.9470-11T>G	XP_011509486.1:n.9470-11T>G