Canonical Allele Identifier: CA1952380

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169128696G>A , CM000664.2:g.169128696G>A	GRCh38
NC_000002.11:g.169985206G>A , CM000664.1:g.169985206G>A	GRCh37
NC_000002.10:g.169693452G>A	NCBI36
NG_012634.1:g.238917C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13935C>T MANE Select	ENSP00000496870.1:p.Thr4645=
ENST00000649153.1:c.4744C>T
ENST00000650252.1:c.2926C>T	ENSP00000496887.1:n.2926C>T
ENST00000263816.7:c.13935C>T	ENSP00000263816.3:p.Thr4645=
NM_004525.2:c.13935C>T	NP_004516.2:p.Thr4645=
XM_011511183.1:c.13806C>T	XP_011509485.1:p.Thr4602=
XM_011511184.1:c.11646C>T	XP_011509486.1:p.Thr3882=
NM_004525.3:c.13935C>T MANE Select	NP_004516.2:p.Thr4645=
XM_011511183.3:c.13806C>T	XP_011509485.1:p.Thr4602=
XM_011511184.2:c.11646C>T	XP_011509486.1:p.Thr3882=