Canonical Allele Identifier: CA59909837
Community Standard Title: NM_004525.3(LRP2):c.10769-147A>G
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169174311T>C , CM000664.2:g.169174311T>C GRCh38
NC_000002.11:g.170030821T>C , CM000664.1:g.170030821T>C GRCh37
NC_000002.10:g.169739067T>C NCBI36
NG_012634.1:g.193302A>G

Transcript Alleles

HGVS Amino-acid Change
NM_004525.3:c.10769-147A>G MANE Select NP_004516.2:n.10769-147A>G
ENST00000649046.1:c.10769-147A>G MANE Select ENSP00000496870.1:n.10769-147A>G
NM_004525.2:c.10769-147A>G NP_004516.2:n.10769-147A>G
ENST00000263816.7:c.10769-147A>G ENSP00000263816.3:n.10769-147A>G
ENST00000649153.1:c.1669-147A>G
XM_011511183.1:c.10769-147A>G XP_011509485.1:n.10769-147A>G
XM_011511183.3:c.10769-147A>G XP_011509485.1:n.10769-147A>G
XM_011511184.1:c.8480-147A>G XP_011509486.1:n.8480-147A>G
XM_011511184.2:c.8480-147A>G XP_011509486.1:n.8480-147A>G