Canonical Allele Identifier: CA349137410

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170011062T>C (hg19) ; chr2:g.169154552T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154552T>C , CM000664.2:g.169154552T>C	GRCh38
NC_000002.11:g.170011062T>C , CM000664.1:g.170011062T>C	GRCh37
NC_000002.10:g.169719308T>C	NCBI36
NG_012634.1:g.213061A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12203A>G MANE Select	ENSP00000496870.1:p.Asn4068Ser
ENST00000649153.1:c.3103A>G
ENST00000650252.1:c.1231A>G	ENSP00000496887.1:p.Ile411Val
ENST00000263816.7:c.12203A>G	ENSP00000263816.3:p.Asn4068Ser
NM_004525.2:c.12203A>G	NP_004516.2:p.Asn4068Ser
XM_011511183.1:c.12074A>G	XP_011509485.1:p.Asn4025Ser
XM_011511184.1:c.9914A>G	XP_011509486.1:p.Asn3305Ser
NM_004525.3:c.12203A>G MANE Select	NP_004516.2:p.Asn4068Ser
XM_011511183.3:c.12074A>G	XP_011509485.1:p.Asn4025Ser
XM_011511184.2:c.9914A>G	XP_011509486.1:p.Asn3305Ser