Canonical Allele Identifier: CA429922562

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170011010T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154500T>C , CM000664.2:g.169154500T>C	GRCh38
NC_000002.11:g.170011010T>C , CM000664.1:g.170011010T>C	GRCh37
NC_000002.10:g.169719256T>C	NCBI36
NG_012634.1:g.213113A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000649046.1:c.12255A>G MANE Select	ENSP00000496870.1:p.Gln4085=
ENST00000649153.1:c.3155A>G
ENST00000650252.1:c.1283A>G	ENSP00000496887.1:p.Lys428Arg
ENST00000263816.7:c.12255A>G	ENSP00000263816.3:p.Gln4085=
NM_004525.2:c.12255A>G	NP_004516.2:p.Gln4085=
XM_011511183.1:c.12126A>G	XP_011509485.1:p.Gln4042=
XM_011511184.1:c.9966A>G	XP_011509486.1:p.Gln3322=
NM_004525.3:c.12255A>G MANE Select	NP_004516.2:p.Gln4085=
XM_011511183.3:c.12126A>G	XP_011509485.1:p.Gln4042=
XM_011511184.2:c.9966A>G	XP_011509486.1:p.Gln3322=