Canonical Allele Identifier: CA349136902

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170010972A>C (hg19) ; chr2:g.169154462A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154462A>C , CM000664.2:g.169154462A>C	GRCh38
NC_000002.11:g.170010972A>C , CM000664.1:g.170010972A>C	GRCh37
NC_000002.10:g.169719218A>C	NCBI36
NG_012634.1:g.213151T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12293T>G MANE Select	ENSP00000496870.1:p.Leu4098Arg
ENST00000649153.1:c.3193T>G
ENST00000650252.1:c.1321T>G	ENSP00000496887.1:n.1321T>G
ENST00000263816.7:c.12293T>G	ENSP00000263816.3:p.Leu4098Arg
NM_004525.2:c.12293T>G	NP_004516.2:p.Leu4098Arg
XM_011511183.1:c.12164T>G	XP_011509485.1:p.Leu4055Arg
XM_011511184.1:c.10004T>G	XP_011509486.1:p.Leu3335Arg
NM_004525.3:c.12293T>G MANE Select	NP_004516.2:p.Leu4098Arg
XM_011511183.3:c.12164T>G	XP_011509485.1:p.Leu4055Arg
XM_011511184.2:c.10004T>G	XP_011509486.1:p.Leu3335Arg