Canonical Allele Identifier: CA3387291
Community Standard Title: NM_001375405.1(CEP120):c.303C>T (p.Thr101=)
Gene: CEP120 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.123416028G>A , CM000667.2:g.123416028G>A GRCh38
NC_000005.9:g.122751722G>A , CM000667.1:g.122751722G>A GRCh37
NC_000005.8:g.122779621G>A NCBI36
NG_042125.1:g.12565C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001375405.1:c.303C>T MANE Select NP_001362334.1:p.Thr101=
ENST00000306467.10:c.303C>T MANE Select ENSP00000303058.6:p.Thr101=
NM_001166226.1:c.225C>T NP_001159698.1:p.Thr75=
NM_001166226.2:c.225C>T NP_001159698.1:p.Thr75=
NM_001375406.1:c.303C>T NP_001362335.1:p.Thr101=
NM_001375407.1:c.303C>T NP_001362336.1:p.Thr101=
NM_001375408.1:c.-446C>T NP_001362337.1:n.-446C>T
NM_001375409.1:c.-388C>T NP_001362338.1:n.-388C>T
NM_153223.3:c.303C>T NP_694955.2:p.Thr101=
NM_153223.4:c.303C>T NP_694955.2:p.Thr101=
NR_164685.1:n.708C>T
ENST00000306467.9:c.303C>T ENSP00000303058.5:p.Thr101=
ENST00000306481.10:c.225C>T ENSP00000307419.6:p.Thr75=
ENST00000306481.11:c.225C>T ENSP00000307419.6:p.Thr75=
ENST00000328236.10:c.303C>T ENSP00000327504.5:p.Thr101=
ENST00000328236.9:c.303C>T ENSP00000327504.5:p.Thr101=
ENST00000503049.2:n.358C>T
ENST00000508138.5:c.303C>T ENSP00000422234.1:p.Thr101=
ENST00000508442.6:c.225C>T ENSP00000421620.2:p.Thr75=
ENST00000508442.7:c.225C>T ENSP00000421620.3:p.Thr75=
ENST00000510582.3:c.303C>T ENSP00000422382.3:p.Thr101=
ENST00000513565.6:c.303C>T ENSP00000422089.2:p.Thr101=
ENST00000674620.1:c.303C>T ENSP00000501651.1:p.Thr101=
ENST00000674667.1:c.303C>T ENSP00000502819.1:p.Thr101=
ENST00000674684.1:c.303C>T ENSP00000501697.1:p.Thr101=
ENST00000675104.1:c.303C>T ENSP00000502078.1:p.Thr101=
ENST00000675330.1:c.303C>T ENSP00000502634.1:p.Thr101=
ENST00000675409.1:n.753C>T
ENST00000675442.1:c.225C>T ENSP00000502221.1:p.Thr75=
ENST00000675444.1:n.726C>T
ENST00000675686.1:c.*199C>T ENSP00000501801.1:n.*199C>T
ENST00000675814.1:c.303C>T ENSP00000502121.1:p.Thr101=
XM_005271901.3:c.303C>T XP_005271958.1:p.Thr101=
XM_005271901.5:c.303C>T XP_005271958.1:p.Thr101=
XM_011543185.1:c.225C>T XP_011541487.1:p.Thr75=
XM_011543185.2:c.225C>T XP_011541487.1:p.Thr75=
XM_024454370.1:c.303C>T XP_024310138.1:p.Thr101=