Canonical Allele Identifier: CA2661815100
Gene: LRP2 HGNC NCBI

Linked Data

gnomAD v4: 2-169154371-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169154371C>T , CM000664.2:g.169154371C>T GRCh38
NC_000002.11:g.170010881C>T , CM000664.1:g.170010881C>T GRCh37
NC_000002.10:g.169719127C>T NCBI36
NG_012634.1:g.213242G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.12295+89G>A MANE Select ENSP00000496870.1:n.12295+89G>A
ENST00000649153.1:c.3195+89G>A
ENST00000650252.1:c.1323+89G>A ENSP00000496887.1:n.1323+89G>A
ENST00000263816.7:c.12295+89G>A ENSP00000263816.3:n.12295+89G>A
NM_004525.2:c.12295+89G>A NP_004516.2:n.12295+89G>A
XM_011511183.1:c.12166+89G>A XP_011509485.1:n.12166+89G>A
XM_011511184.1:c.10006+89G>A XP_011509486.1:n.10006+89G>A
NM_004525.3:c.12295+89G>A MANE Select NP_004516.2:n.12295+89G>A
XM_011511183.3:c.12166+89G>A XP_011509485.1:n.12166+89G>A
XM_011511184.2:c.10006+89G>A XP_011509486.1:n.10006+89G>A
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