Canonical Allele Identifier: CA349137013

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170010989A>C (hg19) ; chr2:g.169154479A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154479A>C , CM000664.2:g.169154479A>C	GRCh38
NC_000002.11:g.170010989A>C , CM000664.1:g.170010989A>C	GRCh37
NC_000002.10:g.169719235A>C	NCBI36
NG_012634.1:g.213134T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12276T>G MANE Select	ENSP00000496870.1:p.Asp4092Glu
ENST00000649153.1:c.3176T>G
ENST00000650252.1:c.1304T>G	ENSP00000496887.1:p.Ile435Ser
ENST00000263816.7:c.12276T>G	ENSP00000263816.3:p.Asp4092Glu
NM_004525.2:c.12276T>G	NP_004516.2:p.Asp4092Glu
XM_011511183.1:c.12147T>G	XP_011509485.1:p.Asp4049Glu
XM_011511184.1:c.9987T>G	XP_011509486.1:p.Asp3329Glu
NM_004525.3:c.12276T>G MANE Select	NP_004516.2:p.Asp4092Glu
XM_011511183.3:c.12147T>G	XP_011509485.1:p.Asp4049Glu
XM_011511184.2:c.9987T>G	XP_011509486.1:p.Asp3329Glu