Canonical Allele Identifier: CA349136974

Gene: LRP2

Linked Data

• dbSNP Id: rs750609040
• gnomAD v3: 2-169154473-C-A
• gnomAD v4: 2-169154473-C-A
• MyVariant Identifiers: chr2:g.170010983C>A (hg19) ; chr2:g.169154473C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154473C>A , CM000664.2:g.169154473C>A	GRCh38
NC_000002.11:g.170010983C>A , CM000664.1:g.170010983C>A	GRCh37
NC_000002.10:g.169719229C>A	NCBI36
NG_012634.1:g.213140G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12282G>T MANE Select	ENSP00000496870.1:p.Lys4094Asn
ENST00000649153.1:c.3182G>T
ENST00000650252.1:c.1310G>T	ENSP00000496887.1:p.Arg437Met
ENST00000263816.7:c.12282G>T	ENSP00000263816.3:p.Lys4094Asn
NM_004525.2:c.12282G>T	NP_004516.2:p.Lys4094Asn
XM_011511183.1:c.12153G>T	XP_011509485.1:p.Lys4051Asn
XM_011511184.1:c.9993G>T	XP_011509486.1:p.Lys3331Asn
NM_004525.3:c.12282G>T MANE Select	NP_004516.2:p.Lys4094Asn
XM_011511183.3:c.12153G>T	XP_011509485.1:p.Lys4051Asn
XM_011511184.2:c.9993G>T	XP_011509486.1:p.Lys3331Asn