Canonical Allele Identifier: CA1039059967

Gene: LRP2

Linked Data

• dbSNP Id: rs779610810
• gnomAD v3: 2-169128985-T-A
• gnomAD v4: 2-169128985-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169128985T>A , CM000664.2:g.169128985T>A	GRCh38
NC_000002.11:g.169985495T>A , CM000664.1:g.169985495T>A	GRCh37
NC_000002.10:g.169693741T>A	NCBI36
NG_012634.1:g.238628A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649046.1:c.13800+28A>T MANE Select	ENSP00000496870.1:n.13800+28A>T
ENST00000649153.1:c.4609+28A>T
ENST00000650252.1:c.2791+28A>T	ENSP00000496887.1:n.2791+28A>T
ENST00000263816.7:c.13800+28A>T	ENSP00000263816.3:n.13800+28A>T
NM_004525.2:c.13800+28A>T	NP_004516.2:n.13800+28A>T
XM_011511183.1:c.13671+28A>T	XP_011509485.1:n.13671+28A>T
XM_011511184.1:c.11511+28A>T	XP_011509486.1:n.11511+28A>T
NM_004525.3:c.13800+28A>T MANE Select	NP_004516.2:n.13800+28A>T
XM_011511183.3:c.13671+28A>T	XP_011509485.1:n.13671+28A>T
XM_011511184.2:c.11511+28A>T	XP_011509486.1:n.11511+28A>T