Canonical Allele Identifier: CA1578889604

Gene: CEP120

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.123349434A= , CM000667.2:g.123349434A=	GRCh38
NC_000005.9:g.122685128A= , CM000667.1:g.122685128A=	GRCh37
NC_000005.8:g.122713027A=	NCBI36
NG_042125.1:g.79159T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306467.10:c.2726+510T= MANE Select	ENSP00000303058.6:n.2726+510T=
ENST00000306481.11:c.2648+510T=	ENSP00000307419.6:n.2648+510T=
ENST00000328236.10:c.2726+510T=	ENSP00000327504.5:n.2726+510T=
ENST00000508442.7:c.2648+510T=	ENSP00000421620.3:n.2648+510T=
ENST00000674620.1:c.*2077+510T=	ENSP00000501651.1:n.*2077+510T=
ENST00000674667.1:c.*1387+510T=	ENSP00000502819.1:n.*1387+510T=
ENST00000674684.1:c.2726+510T=	ENSP00000501697.1:n.2726+510T=
ENST00000675003.1:n.3224+510T=
ENST00000675104.1:c.*1387+510T=	ENSP00000502078.1:n.*1387+510T=
ENST00000675283.1:n.2561+510T=
ENST00000675330.1:c.2591+510T=	ENSP00000502634.1:n.2591+510T=
ENST00000675442.1:c.2627+510T=	ENSP00000502221.1:n.2627+510T=
ENST00000675564.1:n.446+510T=
ENST00000675686.1:c.*2622+510T=	ENSP00000501801.1:n.*2622+510T=
ENST00000675814.1:c.*2279+510T=	ENSP00000502121.1:n.*2279+510T=
ENST00000675852.1:n.4597+510T=
ENST00000676068.1:n.1280+510T=
ENST00000676384.1:n.2633+510T=
ENST00000306467.9:c.2726+510T=	ENSP00000303058.5:n.2726+510T=
ENST00000306481.10:c.2648+510T=	ENSP00000307419.6:n.2648+510T=
ENST00000328236.9:c.2726+510T=	ENSP00000327504.5:n.2726+510T=
ENST00000508138.5:c.*2298+510T=	ENSP00000422234.1:n.*2298+510T=
ENST00000513565.6:c.*2130+510T=	ENSP00000422089.2:n.*2130+510T=
NM_001166226.1:c.2648+510T=	NP_001159698.1:n.2648+510T=
NM_153223.3:c.2726+510T=	NP_694955.2:n.2726+510T=
XM_005271901.3:c.2591+510T=	XP_005271958.1:n.2591+510T=
XM_011543185.1:c.2648+510T=	XP_011541487.1:n.2648+510T=
XM_011543186.1:c.1259+510T=	XP_011541488.1:n.1259+510T=
XM_005271901.5:c.2591+510T=	XP_005271958.1:n.2591+510T=
XM_011543185.2:c.2648+510T=	XP_011541487.1:n.2648+510T=
XM_011543186.2:c.1259+510T=	XP_011541488.1:n.1259+510T=
XM_017009085.1:c.1259+510T=	XP_016864574.1:n.1259+510T=
XM_024454370.1:c.2726+510T=	XP_024310138.1:n.2726+510T=
NM_001375405.1:c.2726+510T= MANE Select	NP_001362334.1:n.2726+510T=
NM_001375406.1:c.2591+510T=	NP_001362335.1:n.2591+510T=
NM_001375407.1:c.2726+510T=	NP_001362336.1:n.2726+510T=
NM_001375408.1:c.2153+510T=	NP_001362337.1:n.2153+510T=
NM_001375409.1:c.2153+510T=	NP_001362338.1:n.2153+510T=
NR_164685.1:n.3678+510T=
NM_001166226.2:c.2648+510T=	NP_001159698.1:n.2648+510T=
NM_153223.4:c.2726+510T=	NP_694955.2:n.2726+510T=