Canonical Allele Identifier: CA429922606

Gene: LRP2

Linked Data

• MyVariant Identifiers: chr2:g.170011078G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169154568G>T , CM000664.2:g.169154568G>T	GRCh38
NC_000002.11:g.170011078G>T , CM000664.1:g.170011078G>T	GRCh37
NC_000002.10:g.169719324G>T	NCBI36
NG_012634.1:g.213045C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.12187C>A MANE Select	ENSP00000496870.1:p.Arg4063=
ENST00000649153.1:c.3087C>A
ENST00000650252.1:c.1215C>A	ENSP00000496887.1:p.Ser405=
ENST00000263816.7:c.12187C>A	ENSP00000263816.3:p.Arg4063=
NM_004525.2:c.12187C>A	NP_004516.2:p.Arg4063=
XM_011511183.1:c.12058C>A	XP_011509485.1:p.Arg4020=
XM_011511184.1:c.9898C>A	XP_011509486.1:p.Arg3300=
NM_004525.3:c.12187C>A MANE Select	NP_004516.2:p.Arg4063=
XM_011511183.3:c.12058C>A	XP_011509485.1:p.Arg4020=
XM_011511184.2:c.9898C>A	XP_011509486.1:p.Arg3300=