Canonical Allele Identifier: CA349137268

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170011030G>T (hg19) ; chr2:g.169154520G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154520G>T , CM000664.2:g.169154520G>T	GRCh38
NC_000002.11:g.170011030G>T , CM000664.1:g.170011030G>T	GRCh37
NC_000002.10:g.169719276G>T	NCBI36
NG_012634.1:g.213093C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12235C>A MANE Select	ENSP00000496870.1:p.Gln4079Lys
ENST00000649153.1:c.3135C>A
ENST00000650252.1:c.1263C>A	ENSP00000496887.1:p.Phe421Leu
ENST00000263816.7:c.12235C>A	ENSP00000263816.3:p.Gln4079Lys
NM_004525.2:c.12235C>A	NP_004516.2:p.Gln4079Lys
XM_011511183.1:c.12106C>A	XP_011509485.1:p.Gln4036Lys
XM_011511184.1:c.9946C>A	XP_011509486.1:p.Gln3316Lys
NM_004525.3:c.12235C>A MANE Select	NP_004516.2:p.Gln4079Lys
XM_011511183.3:c.12106C>A	XP_011509485.1:p.Gln4036Lys
XM_011511184.2:c.9946C>A	XP_011509486.1:p.Gln3316Lys