Canonical Allele Identifier: CA1306305589
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154498G= , CM000664.2:g.169154498G= GRCh38
NC_000002.11:g.170011008G= , CM000664.1:g.170011008G= GRCh37
NC_000002.10:g.169719254G= NCBI36
NG_012634.1:g.213115C=

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12257C= MANE Select ENSP00000496870.1:p.Ala4086=
ENST00000649153.1:c.3157C=
ENST00000650252.1:c.1285C= ENSP00000496887.1:p.Leu429=
ENST00000263816.7:c.12257C= ENSP00000263816.3:p.Ala4086=
NM_004525.2:c.12257C= NP_004516.2:p.Ala4086=
XM_011511183.1:c.12128C= XP_011509485.1:p.Ala4043=
XM_011511184.1:c.9968C= XP_011509486.1:p.Ala3323=
NM_004525.3:c.12257C= MANE Select NP_004516.2:p.Ala4086=
XM_011511183.3:c.12128C= XP_011509485.1:p.Ala4043=
XM_011511184.2:c.9968C= XP_011509486.1:p.Ala3323=