Canonical Allele Identifier: CA349149489

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.169985582T>C (hg19) ; chr2:g.169129072T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169129072T>C , CM000664.2:g.169129072T>C	GRCh38
NC_000002.11:g.169985582T>C , CM000664.1:g.169985582T>C	GRCh37
NC_000002.10:g.169693828T>C	NCBI36
NG_012634.1:g.238541A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13741A>G MANE Select	ENSP00000496870.1:p.Asn4581Asp
ENST00000649153.1:c.4550A>G
ENST00000650252.1:c.2732A>G	ENSP00000496887.1:n.2732A>G
ENST00000263816.7:c.13741A>G	ENSP00000263816.3:p.Asn4581Asp
NM_004525.2:c.13741A>G	NP_004516.2:p.Asn4581Asp
XM_011511183.1:c.13612A>G	XP_011509485.1:p.Asn4538Asp
XM_011511184.1:c.11452A>G	XP_011509486.1:p.Asn3818Asp
NM_004525.3:c.13741A>G MANE Select	NP_004516.2:p.Asn4581Asp
XM_011511183.3:c.13612A>G	XP_011509485.1:p.Asn4538Asp
XM_011511184.2:c.11452A>G	XP_011509486.1:p.Asn3818Asp