Canonical Allele Identifier: CA429922566

Gene: LRP2

Linked Data

• gnomAD v4: 2-169154509-T-C
• MyVariant Identifiers: chr2:g.170011019T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154509T>C , CM000664.2:g.169154509T>C	GRCh38
NC_000002.11:g.170011019T>C , CM000664.1:g.170011019T>C	GRCh37
NC_000002.10:g.169719265T>C	NCBI36
NG_012634.1:g.213104A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12246A>G MANE Select	ENSP00000496870.1:p.Glu4082=
ENST00000649153.1:c.3146A>G
ENST00000650252.1:c.1274A>G	ENSP00000496887.1:p.Asn425Ser
ENST00000263816.7:c.12246A>G	ENSP00000263816.3:p.Glu4082=
NM_004525.2:c.12246A>G	NP_004516.2:p.Glu4082=
XM_011511183.1:c.12117A>G	XP_011509485.1:p.Glu4039=
XM_011511184.1:c.9957A>G	XP_011509486.1:p.Glu3319=
NM_004525.3:c.12246A>G MANE Select	NP_004516.2:p.Glu4082=
XM_011511183.3:c.12117A>G	XP_011509485.1:p.Glu4039=
XM_011511184.2:c.9957A>G	XP_011509486.1:p.Glu3319=