Canonical Allele Identifier: CA349149401
Gene: LRP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169129061T>A , CM000664.2:g.169129061T>A GRCh38
NC_000002.11:g.169985571T>A , CM000664.1:g.169985571T>A GRCh37
NC_000002.10:g.169693817T>A NCBI36
NG_012634.1:g.238552A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.13752A>T MANE Select ENSP00000496870.1:p.Lys4584Asn
ENST00000649153.1:c.4561A>T
ENST00000650252.1:c.2743A>T ENSP00000496887.1:n.2743A>T
ENST00000263816.7:c.13752A>T ENSP00000263816.3:p.Lys4584Asn
NM_004525.2:c.13752A>T NP_004516.2:p.Lys4584Asn
XM_011511183.1:c.13623A>T XP_011509485.1:p.Lys4541Asn
XM_011511184.1:c.11463A>T XP_011509486.1:p.Lys3821Asn
NM_004525.3:c.13752A>T MANE Select NP_004516.2:p.Lys4584Asn
XM_011511183.3:c.13623A>T XP_011509485.1:p.Lys4541Asn
XM_011511184.2:c.11463A>T XP_011509486.1:p.Lys3821Asn