Canonical Allele Identifier: CA360891224
Gene: CEP120 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.123390060C>A , CM000667.2:g.123390060C>A GRCh38
NC_000005.9:g.122725754C>A , CM000667.1:g.122725754C>A GRCh37
NC_000005.8:g.122753653C>A NCBI36
NG_042125.1:g.38533G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306467.10:c.1119G>T MANE Select ENSP00000303058.6:p.Lys373Asn
ENST00000306481.11:c.1041G>T ENSP00000307419.6:p.Lys347Asn
ENST00000328236.10:c.1119G>T ENSP00000327504.5:p.Lys373Asn
ENST00000503049.2:n.1174G>T
ENST00000508442.7:c.1041G>T ENSP00000421620.3:p.Lys347Asn
ENST00000674620.1:c.*525-55G>T ENSP00000501651.1:n.*525-55G>T
ENST00000674667.1:c.1119G>T ENSP00000502819.1:p.Lys373Asn
ENST00000674684.1:c.1119G>T ENSP00000501697.1:p.Lys373Asn
ENST00000675003.1:n.1489G>T
ENST00000675104.1:c.1039-55G>T ENSP00000502078.1:n.1039-55G>T
ENST00000675283.1:n.954G>T
ENST00000675330.1:c.1039-55G>T ENSP00000502634.1:n.1039-55G>T
ENST00000675409.1:n.1569G>T
ENST00000675442.1:c.1041G>T ENSP00000502221.1:p.Lys347Asn
ENST00000675444.1:n.1542G>T
ENST00000675686.1:c.*1015G>T ENSP00000501801.1:n.*1015G>T
ENST00000675814.1:c.*672G>T ENSP00000502121.1:n.*672G>T
ENST00000675852.1:n.2990G>T
ENST00000306467.9:c.1119G>T ENSP00000303058.5:p.Lys373Asn
ENST00000306481.10:c.1041G>T ENSP00000307419.6:p.Lys347Asn
ENST00000328236.9:c.1119G>T ENSP00000327504.5:p.Lys373Asn
ENST00000508138.5:c.*691G>T ENSP00000422234.1:n.*691G>T
ENST00000508442.6:c.1041G>T ENSP00000421620.2:p.Lys347Asn
ENST00000513565.6:c.*201G>T ENSP00000422089.2:n.*201G>T
NM_001166226.1:c.1041G>T NP_001159698.1:p.Lys347Asn
NM_153223.3:c.1119G>T NP_694955.2:p.Lys373Asn
XM_005271901.3:c.1039-55G>T XP_005271958.1:n.1039-55G>T
XM_011543185.1:c.1041G>T XP_011541487.1:p.Lys347Asn
XM_005271901.5:c.1039-55G>T XP_005271958.1:n.1039-55G>T
XM_011543185.2:c.1041G>T XP_011541487.1:p.Lys347Asn
XM_011543186.2:c.-477G>T XP_011541488.1:n.-477G>T
XM_017009085.1:c.-422-55G>T XP_016864574.1:n.-422-55G>T
XM_024454370.1:c.1119G>T XP_024310138.1:p.Lys373Asn
NM_001375405.1:c.1119G>T MANE Select NP_001362334.1:p.Lys373Asn
NM_001375406.1:c.1039-55G>T NP_001362335.1:n.1039-55G>T
NM_001375407.1:c.1119G>T NP_001362336.1:p.Lys373Asn
NM_001375408.1:c.546G>T NP_001362337.1:p.Lys182Asn
NM_001375409.1:c.546G>T NP_001362338.1:p.Lys182Asn
NR_164685.1:n.1749G>T
NM_001166226.2:c.1041G>T NP_001159698.1:p.Lys347Asn
NM_153223.4:c.1119G>T NP_694955.2:p.Lys373Asn