Canonical Allele Identifier: CA2577150237
Gene: LRP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169247614T>A , CM000664.2:g.169247614T>A GRCh38
NC_000002.11:g.170104124T>A , CM000664.1:g.170104124T>A GRCh37
NC_000002.10:g.169812370T>A NCBI36
NG_012634.1:g.119999A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649046.1:c.2771-99A>T MANE Select ENSP00000496870.1:n.2771-99A>T
ENST00000263816.7:c.2771-99A>T ENSP00000263816.3:n.2771-99A>T
ENST00000443831.1:c.2360-99A>T ENSP00000409813.1:n.2360-99A>T
NM_004525.2:c.2771-99A>T NP_004516.2:n.2771-99A>T
XM_011511183.1:c.2771-99A>T XP_011509485.1:n.2771-99A>T
XM_011511184.1:c.482-99A>T XP_011509486.1:n.482-99A>T
XM_011511185.1:c.2771-99A>T XP_011509487.1:n.2771-99A>T
NM_004525.3:c.2771-99A>T MANE Select NP_004516.2:n.2771-99A>T
XM_011511183.3:c.2771-99A>T XP_011509485.1:n.2771-99A>T
XM_011511184.2:c.482-99A>T XP_011509486.1:n.482-99A>T