Canonical Allele Identifier: CA349150695

Gene: LRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169132600T>A , CM000664.2:g.169132600T>A	GRCh38
NC_000002.11:g.169989110T>A , CM000664.1:g.169989110T>A	GRCh37
NC_000002.10:g.169697356T>A	NCBI36
NG_012634.1:g.235013A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13702A>T MANE Select	ENSP00000496870.1:p.Thr4568Ser
ENST00000649153.1:c.4511A>T
ENST00000650252.1:c.2693A>T	ENSP00000496887.1:n.2693A>T
ENST00000263816.7:c.13702A>T	ENSP00000263816.3:p.Thr4568Ser
ENST00000491228.1:n.556A>T
NM_004525.2:c.13702A>T	NP_004516.2:p.Thr4568Ser
XM_011511183.1:c.13573A>T	XP_011509485.1:p.Thr4525Ser
XM_011511184.1:c.11413A>T	XP_011509486.1:p.Thr3805Ser
NM_004525.3:c.13702A>T MANE Select	NP_004516.2:p.Thr4568Ser
XM_011511183.3:c.13573A>T	XP_011509485.1:p.Thr4525Ser
XM_011511184.2:c.11413A>T	XP_011509486.1:p.Thr3805Ser