Canonical Allele Identifier: CA125978285

Gene: CEP120

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.123391252T>C , CM000667.2:g.123391252T>C	GRCh38
NC_000005.9:g.122726946T>C , CM000667.1:g.122726946T>C	GRCh37
NC_000005.8:g.122754845T>C	NCBI36
NG_042125.1:g.37341A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306467.10:c.896A>G MANE Select	ENSP00000303058.6:p.Asn299Ser
ENST00000306481.11:c.818A>G	ENSP00000307419.6:p.Asn273Ser
ENST00000328236.10:c.896A>G	ENSP00000327504.5:p.Asn299Ser
ENST00000503049.2:n.951A>G
ENST00000508442.7:c.818A>G	ENSP00000421620.3:p.Asn273Ser
ENST00000674620.1:c.*382A>G	ENSP00000501651.1:n.*382A>G
ENST00000674667.1:c.896A>G	ENSP00000502819.1:p.Asn299Ser
ENST00000674684.1:c.896A>G	ENSP00000501697.1:p.Asn299Ser
ENST00000675003.1:n.1266A>G
ENST00000675104.1:c.896A>G	ENSP00000502078.1:p.Asn299Ser
ENST00000675283.1:n.731A>G
ENST00000675330.1:c.896A>G	ENSP00000502634.1:p.Asn299Ser
ENST00000675409.1:n.1346A>G
ENST00000675442.1:c.818A>G	ENSP00000502221.1:p.Asn273Ser
ENST00000675444.1:n.1319A>G
ENST00000675686.1:c.*792A>G	ENSP00000501801.1:n.*792A>G
ENST00000675814.1:c.*449A>G	ENSP00000502121.1:n.*449A>G
ENST00000675852.1:n.1798A>G
ENST00000306467.9:c.896A>G	ENSP00000303058.5:p.Asn299Ser
ENST00000306481.10:c.818A>G	ENSP00000307419.6:p.Asn273Ser
ENST00000328236.9:c.896A>G	ENSP00000327504.5:p.Asn299Ser
ENST00000503049.1:n.236A>G
ENST00000508138.5:c.*468A>G	ENSP00000422234.1:n.*468A>G
ENST00000508442.6:c.818A>G	ENSP00000421620.2:p.Asn273Ser
ENST00000513565.6:c.896A>G	ENSP00000422089.2:p.Asn299Ser
NM_001166226.1:c.818A>G	NP_001159698.1:p.Asn273Ser
NM_153223.3:c.896A>G	NP_694955.2:p.Asn299Ser
XM_005271901.3:c.896A>G	XP_005271958.1:p.Asn299Ser
XM_011543185.1:c.818A>G	XP_011541487.1:p.Asn273Ser
XM_005271901.5:c.896A>G	XP_005271958.1:p.Asn299Ser
XM_011543185.2:c.818A>G	XP_011541487.1:p.Asn273Ser
XM_011543186.2:c.-700A>G	XP_011541488.1:n.-700A>G
XM_017009085.1:c.-565A>G	XP_016864574.1:n.-565A>G
XM_024454370.1:c.896A>G	XP_024310138.1:p.Asn299Ser
NM_001375405.1:c.896A>G MANE Select	NP_001362334.1:p.Asn299Ser
NM_001375406.1:c.896A>G	NP_001362335.1:p.Asn299Ser
NM_001375407.1:c.896A>G	NP_001362336.1:p.Asn299Ser
NM_001375408.1:c.323A>G	NP_001362337.1:p.Asn108Ser
NM_001375409.1:c.323A>G	NP_001362338.1:p.Asn108Ser
NR_164685.1:n.1301A>G
NM_001166226.2:c.818A>G	NP_001159698.1:p.Asn273Ser
NM_153223.4:c.896A>G	NP_694955.2:p.Asn299Ser