Canonical Allele Identifier: CA429917566

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169132658A>G , CM000664.2:g.169132658A>G	GRCh38
NC_000002.11:g.169989168A>G , CM000664.1:g.169989168A>G	GRCh37
NC_000002.10:g.169697414A>G	NCBI36
NG_012634.1:g.234955T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13644T>C MANE Select	ENSP00000496870.1:p.Asp4548=
ENST00000649153.1:c.4453T>C
ENST00000650252.1:c.2635T>C	ENSP00000496887.1:n.2635T>C
ENST00000263816.7:c.13644T>C	ENSP00000263816.3:p.Asp4548=
ENST00000491228.1:n.498T>C
NM_004525.2:c.13644T>C	NP_004516.2:p.Asp4548=
XM_011511183.1:c.13515T>C	XP_011509485.1:p.Asp4505=
XM_011511184.1:c.11355T>C	XP_011509486.1:p.Asp3785=
NM_004525.3:c.13644T>C MANE Select	NP_004516.2:p.Asp4548=
XM_011511183.3:c.13515T>C	XP_011509485.1:p.Asp4505=
XM_011511184.2:c.11355T>C	XP_011509486.1:p.Asp3785=