Canonical Allele Identifier: CA14557625
Gene: LDLRAD4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13366863A>G , CM000680.2:g.13366863A>G GRCh38
NC_000018.9:g.13366862A>G , CM000680.1:g.13366862A>G GRCh37
NC_000018.8:g.13356862A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359446.11:c.-382-20478A>G MANE Select ENSP00000352420.5:n.-382-20478A>G
ENST00000359446.10:c.-382-20478A>G ENSP00000352420.5:n.-382-20478A>G
ENST00000587905.6:c.-382-20478A>G ENSP00000465244.2:n.-382-20478A>G
ENST00000676672.1:c.-382-20478A>G ENSP00000504500.1:n.-382-20478A>G
ENST00000676891.1:c.-382-20478A>G ENSP00000503092.1:n.-382-20478A>G
ENST00000677055.1:c.-382-20478A>G ENSP00000504396.1:n.-382-20478A>G
ENST00000677304.1:c.-382-20478A>G ENSP00000503549.1:n.-382-20478A>G
ENST00000678459.1:c.-382-20478A>G ENSP00000504668.1:n.-382-20478A>G
ENST00000679091.1:c.-382-20478A>G ENSP00000503185.1:n.-382-20478A>G
ENST00000679167.1:c.-382-20478A>G ENSP00000504651.1:n.-382-20478A>G
ENST00000679177.1:c.-382-20478A>G ENSP00000504217.1:n.-382-20478A>G
ENST00000359446.9:c.-382-20478A>G ENSP00000352420.5:n.-382-20478A>G
ENST00000399848.7:c.-382-20478A>G ENSP00000382741.2:n.-382-20478A>G
ENST00000587905.5:c.-382-20478A>G ENSP00000465244.1:n.-382-20478A>G
ENST00000590371.5:n.362-20478A>G
NM_181481.4:c.-382-20478A>G NP_852146.1:n.-382-20478A>G
NM_181482.4:c.-382-20478A>G NP_852147.1:n.-382-20478A>G
XM_005258140.1:c.-382-20478A>G XP_005258197.1:n.-382-20478A>G
XM_006722353.1:c.-382-20478A>G XP_006722416.1:n.-382-20478A>G
XM_011525737.1:c.-382-20478A>G XP_011524039.1:n.-382-20478A>G
XM_011525738.1:c.-555-20478A>G XP_011524040.1:n.-555-20478A>G
XM_017025961.1:c.-410-20478A>G XP_016881450.1:n.-410-20478A>G
XM_017025962.1:c.-410-20478A>G XP_016881451.1:n.-410-20478A>G
XM_017025963.2:c.-382-20478A>G XP_016881452.1:n.-382-20478A>G
XM_017025964.1:c.-382-20478A>G XP_016881453.1:n.-382-20478A>G
XM_017025965.1:c.-980-20478A>G XP_016881454.1:n.-980-20478A>G
XM_017025966.1:c.-855-20478A>G XP_016881455.1:n.-855-20478A>G
XM_017025967.1:c.-852-20478A>G XP_016881456.1:n.-852-20478A>G
XM_017025968.1:c.-759-20478A>G XP_016881457.1:n.-759-20478A>G
XM_024451248.1:c.-382-20478A>G XP_024307016.1:n.-382-20478A>G
XM_024451249.1:c.-382-20478A>G XP_024307017.1:n.-382-20478A>G
XM_024451250.1:c.-382-20478A>G XP_024307018.1:n.-382-20478A>G
XM_024451251.1:c.-382-20478A>G XP_024307019.1:n.-382-20478A>G
XM_024451252.1:c.-382-20478A>G XP_024307020.1:n.-382-20478A>G
XM_024451253.1:c.-382-20478A>G XP_024307021.1:n.-382-20478A>G
XM_024451254.1:c.-382-20478A>G XP_024307022.1:n.-382-20478A>G
XM_024451255.1:c.-382-20478A>G XP_024307023.1:n.-382-20478A>G
XM_024451256.1:c.-382-20478A>G XP_024307024.1:n.-382-20478A>G
XM_024451257.1:c.-382-20478A>G XP_024307025.1:n.-382-20478A>G
XM_024451259.1:c.-382-20478A>G XP_024307027.1:n.-382-20478A>G
XM_024451260.1:c.-382-20478A>G XP_024307028.1:n.-382-20478A>G
NM_181482.5:c.-382-20478A>G NP_852147.1:n.-382-20478A>G
NM_001378098.1:c.-382-20478A>G NP_001365027.1:n.-382-20478A>G
NM_001378099.1:c.-382-20478A>G NP_001365028.1:n.-382-20478A>G
NM_001378100.1:c.-382-20478A>G MANE Select NP_001365029.1:n.-382-20478A>G
NM_001378101.1:c.-382-20478A>G NP_001365030.1:n.-382-20478A>G
NM_181481.5:c.-382-20478A>G NP_852146.1:n.-382-20478A>G
NM_001394662.1:c.-382-20478A>G NP_001381591.1:n.-382-20478A>G
NM_001394663.1:c.-382-20478A>G NP_001381592.1:n.-382-20478A>G
NM_001394664.1:c.-382-20478A>G NP_001381593.1:n.-382-20478A>G
NM_001394665.1:c.-382-20478A>G NP_001381594.1:n.-382-20478A>G
NM_001394666.1:c.-382-20478A>G NP_001381595.1:n.-382-20478A>G
NM_001394667.1:c.-382-20478A>G NP_001381596.1:n.-382-20478A>G
NR_172142.1:n.208-20478A>G
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