Canonical Allele Identifier: CA695429
Gene: LDLRAP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25553921G>C , CM000663.2:g.25553921G>C GRCh38
NC_000001.10:g.25880412G>C , CM000663.1:g.25880412G>C GRCh37
NC_000001.9:g.25752999G>C NCBI36
NG_008932.1:g.15337G>C , LRG_276:g.15337G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374338.5:c.89-1G>C MANE Select ENSP00000363458.4:n.89-1G>C
ENST00000374338.4:c.89-1G>C ENSP00000363458.4:n.89-1G>C
ENST00000485476.2:n.76-1G>C
ENST00000488127.1:n.558G>C
NM_015627.2:c.89-1G>C , LRG_276t1:c.89-1G>C NP_056442.2:n.89-1G>C
XM_006710559.2:c.89-1G>C XP_006710622.1:n.89-1G>C
XM_006710560.2:c.89-1G>C XP_006710623.1:n.89-1G>C
XM_006710561.2:c.89-1G>C XP_006710624.1:n.89-1G>C
XM_011541209.1:c.89-1G>C XP_011539511.1:n.89-1G>C
XM_011541210.1:c.89-1G>C XP_011539512.1:n.89-1G>C
XM_011541211.1:c.89-1G>C XP_011539513.1:n.89-1G>C
XM_011541212.1:c.89-1G>C XP_011539514.1:n.89-1G>C
XR_426598.2:n.208-1G>C
XR_946602.1:n.208-1G>C
XR_946603.1:n.208-1G>C
XM_006710559.4:c.89-1G>C XP_006710622.1:n.89-1G>C
XM_006710560.4:c.89-1G>C XP_006710623.1:n.89-1G>C
XM_006710561.4:c.89-1G>C XP_006710624.1:n.89-1G>C
XM_011541209.3:c.89-1G>C XP_011539511.1:n.89-1G>C
XM_011541210.3:c.89-1G>C XP_011539512.1:n.89-1G>C
XM_011541211.3:c.89-1G>C XP_011539513.1:n.89-1G>C
XM_011541212.3:c.89-1G>C XP_011539514.1:n.89-1G>C
XM_017000994.2:c.8-1G>C XP_016856483.1:n.8-1G>C
XM_017000995.2:c.89-1G>C XP_016856484.1:n.89-1G>C
XM_024446315.1:c.-47-1G>C XP_024302083.1:n.-47-1G>C
XR_001737112.2:n.159-1G>C
XR_001737113.2:n.159-1G>C
XR_002956258.1:n.159-1G>C
XR_426598.4:n.159-1G>C
XR_946602.3:n.159-1G>C
XR_946603.3:n.159-1G>C
NM_015627.3:c.89-1G>C MANE Select NP_056442.2:n.89-1G>C
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