Canonical Allele Identifier: CA2644169938
Gene: LDLRAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25557277del , CM000663.2:g.25557277del GRCh38
NC_000001.10:g.25883768del , CM000663.1:g.25883768del GRCh37
NC_000001.9:g.25756355del NCBI36
NG_008932.1:g.18693del , LRG_276:g.18693del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374338.5:c.459+10del MANE Select ENSP00000363458.4:n.459+10del
ENST00000374338.4:c.459+10del ENSP00000363458.4:n.459+10del
ENST00000462394.1:n.217del
ENST00000488127.1:n.929+10del
NM_015627.2:c.459+10del , LRG_276t1:c.459+10del NP_056442.2:n.459+10del
XM_006710559.2:c.459+10del XP_006710622.1:n.459+10del
XM_006710560.2:c.459+10del XP_006710623.1:n.459+10del
XM_006710561.2:c.459+10del XP_006710624.1:n.459+10del
XM_011541209.1:c.459+10del XP_011539511.1:n.459+10del
XM_011541210.1:c.459+10del XP_011539512.1:n.459+10del
XM_011541211.1:c.459+10del XP_011539513.1:n.459+10del
XM_011541212.1:c.459+10del XP_011539514.1:n.459+10del
XR_426598.2:n.578+10del
XR_946602.1:n.578+10del
XR_946603.1:n.578+10del
XM_006710559.4:c.459+10del XP_006710622.1:n.459+10del
XM_006710560.4:c.459+10del XP_006710623.1:n.459+10del
XM_006710561.4:c.459+10del XP_006710624.1:n.459+10del
XM_011541209.3:c.459+10del XP_011539511.1:n.459+10del
XM_011541210.3:c.459+10del XP_011539512.1:n.459+10del
XM_011541211.3:c.459+10del XP_011539513.1:n.459+10del
XM_011541212.3:c.459+10del XP_011539514.1:n.459+10del
XM_017000994.2:c.378+10del XP_016856483.1:n.378+10del
XM_017000995.2:c.459+10del XP_016856484.1:n.459+10del
XM_024446315.1:c.324+10del XP_024302083.1:n.324+10del
XR_001737112.2:n.529+10del
XR_001737113.2:n.529+10del
XR_002956258.1:n.529+10del
XR_426598.4:n.529+10del
XR_946602.3:n.529+10del
XR_946603.3:n.529+10del
NM_015627.3:c.459+10del MANE Select NP_056442.2:n.459+10del