Canonical Allele Identifier: CA59905852
Community Standard Title: NM_004525.3(LRP2):c.11636-310A>T
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169166364T>A , CM000664.2:g.169166364T>A GRCh38
NC_000002.11:g.170022874T>A , CM000664.1:g.170022874T>A GRCh37
NC_000002.10:g.169731120T>A NCBI36
NG_012634.1:g.201249A>T

Transcript Alleles

HGVS Amino-acid Change
NM_004525.3:c.11636-310A>T MANE Select NP_004516.2:n.11636-310A>T
ENST00000649046.1:c.11636-310A>T MANE Select ENSP00000496870.1:n.11636-310A>T
NM_004525.2:c.11636-310A>T NP_004516.2:n.11636-310A>T
ENST00000263816.7:c.11636-310A>T ENSP00000263816.3:n.11636-310A>T
ENST00000649153.1:c.2536-310A>T
ENST00000650252.1:c.668-310A>T ENSP00000496887.1:n.668-310A>T
XM_011511183.1:c.11507-310A>T XP_011509485.1:n.11507-310A>T
XM_011511183.3:c.11507-310A>T XP_011509485.1:n.11507-310A>T
XM_011511184.1:c.9347-310A>T XP_011509486.1:n.9347-310A>T
XM_011511184.2:c.9347-310A>T XP_011509486.1:n.9347-310A>T