Canonical Allele Identifier: CA2577150227
Gene: LRP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169247348A>G , CM000664.2:g.169247348A>G GRCh38
NC_000002.11:g.170103858A>G , CM000664.1:g.170103858A>G GRCh37
NC_000002.10:g.169812104A>G NCBI36
NG_012634.1:g.120265T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.2908+30T>C MANE Select ENSP00000496870.1:n.2908+30T>C
ENST00000263816.7:c.2908+30T>C ENSP00000263816.3:n.2908+30T>C
ENST00000443831.1:c.2497+30T>C ENSP00000409813.1:n.2497+30T>C
NM_004525.2:c.2908+30T>C NP_004516.2:n.2908+30T>C
XM_011511183.1:c.2908+30T>C XP_011509485.1:n.2908+30T>C
XM_011511184.1:c.619+30T>C XP_011509486.1:n.619+30T>C
XM_011511185.1:c.2908+30T>C XP_011509487.1:n.2908+30T>C
NM_004525.3:c.2908+30T>C MANE Select NP_004516.2:n.2908+30T>C
XM_011511183.3:c.2908+30T>C XP_011509485.1:n.2908+30T>C
XM_011511184.2:c.619+30T>C XP_011509486.1:n.619+30T>C
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