Canonical Allele Identifier: CA59905498

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169165789T>C , CM000664.2:g.169165789T>C	GRCh38
NC_000002.11:g.170022299T>C , CM000664.1:g.170022299T>C	GRCh37
NC_000002.10:g.169730545T>C	NCBI36
NG_012634.1:g.201824A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004525.3:c.11758+143A>G MANE Select	NP_004516.2:n.11758+143A>G
ENST00000649046.1:c.11758+143A>G MANE Select	ENSP00000496870.1:n.11758+143A>G
NM_004525.2:c.11758+143A>G	NP_004516.2:n.11758+143A>G
ENST00000263816.7:c.11758+143A>G	ENSP00000263816.3:n.11758+143A>G
ENST00000649153.1:c.2658+143A>G
ENST00000650252.1:c.790+143A>G	ENSP00000496887.1:n.790+143A>G
XM_011511183.1:c.11629+143A>G	XP_011509485.1:n.11629+143A>G
XM_011511183.3:c.11629+143A>G	XP_011509485.1:n.11629+143A>G
XM_011511184.1:c.9469+143A>G	XP_011509486.1:n.9469+143A>G
XM_011511184.2:c.9469+143A>G	XP_011509486.1:n.9469+143A>G