Canonical Allele Identifier: CA1306397485
Gene: LRP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169348238C= , CM000664.2:g.169348238C= GRCh38
NC_000002.11:g.170204748C= , CM000664.1:g.170204748C= GRCh37
NC_000002.10:g.169912994C= NCBI36
NG_012634.1:g.19375G=

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.79+14083G= MANE Select ENSP00000496870.1:n.79+14083G=
ENST00000263816.7:c.79+14083G= ENSP00000263816.3:n.79+14083G=
ENST00000443831.1:c.79+14083G= ENSP00000409813.1:n.79+14083G=
NM_004525.2:c.79+14083G= NP_004516.2:n.79+14083G=
XM_011511183.1:c.79+14083G= XP_011509485.1:n.79+14083G=
XM_011511185.1:c.79+14083G= XP_011509487.1:n.79+14083G=
NM_004525.3:c.79+14083G= MANE Select NP_004516.2:n.79+14083G=
XM_011511183.3:c.79+14083G= XP_011509485.1:n.79+14083G=
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