Canonical Allele Identifier: CA1165524839

Gene: CFAP57 EBNA1BP2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43206756_43206757delinsCT , CM000663.2:g.43206756_43206757delinsCT	GRCh38
NC_000001.10:g.43672427_43672428delinsCT , CM000663.1:g.43672427_43672428delinsCT	GRCh37
NC_000001.9:g.43445014_43445015delinsCT	NCBI36
NG_028079.1:g.39427_39428delinsCT
NG_028079.2:g.39427_39428delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372492.9:c.1579_1580delinsCT (CFAP57) MANE Select	ENSP00000361570.4:p.Leu527=
ENST00000372492.8:c.1579_1580delinsCT (CFAP57)	ENSP00000361570.4:p.Leu527=
ENST00000461557.2:n.233+4693_233+4694delinsAG (EBNA1BP2)
ENST00000466927.5:n.197+8509_197+8510delinsAG (EBNA1BP2)
ENST00000474566.1:n.420-365_420-364delinsAG (EBNA1BP2)
ENST00000528956.5:c.1579_1580delinsCT (CFAP57)	ENSP00000435310.1:p.Leu527=
ENST00000533339.1:c.*1478_*1479delinsCT (CFAP57)	ENSP00000432547.1:n.*1478_*1479delinsCT
ENST00000610710.4:c.1579_1580delinsCT (CFAP57)	ENSP00000479773.1:p.Leu527=
NM_001167965.1:c.1579_1580delinsCT (CFAP57)	NP_001161437.1:p.Leu527=
NM_001195831.2:c.1579_1580delinsCT (CFAP57)	NP_001182760.2:p.Leu527=
NM_152498.3:c.1579_1580delinsCT (CFAP57)	NP_689711.2:p.Leu527=
XM_005270520.1:c.1579_1580delinsCT (CFAP57)	XP_005270577.1:p.Leu527=
XM_006710383.1:c.1546_1547delinsCT (CFAP57)	XP_006710446.1:p.Leu516=
XM_011540793.1:c.1579_1580delinsCT (CFAP57)	XP_011539095.1:p.Leu527=
XM_011540794.1:c.1579_1580delinsCT (CFAP57)	XP_011539096.1:p.Leu527=
XM_011540795.1:c.1579_1580delinsCT (CFAP57)	XP_011539097.1:p.Leu527=
XM_011540796.1:c.1546_1547delinsCT (CFAP57)	XP_011539098.1:p.Leu516=
XM_011540797.1:c.1516_1517delinsCT (CFAP57)	XP_011539099.1:p.Leu506=
XM_011540798.1:c.1543-2987_1543-2986delinsCT (CFAP57)	XP_011539100.1:n.1543-2987_1543-2986delinsCT
XM_011540799.1:c.1542+7253_1542+7254delinsCT (CFAP57)	XP_011539101.1:n.1542+7253_1542+7254delinsCT
XM_011540800.1:c.1579_1580delinsCT (CFAP57)	XP_011539102.1:p.Leu527=
XM_011540801.1:c.1579_1580delinsCT (CFAP57)	XP_011539103.1:p.Leu527=
XR_947266.1:n.450-365_450-364delinsAG
XR_947267.1:n.455-365_455-364delinsAG
XR_947268.1:n.240-365_240-364delinsAG
XR_947269.1:n.1064-365_1064-364delinsAG
XR_947270.1:n.214-365_214-364delinsAG
XR_947271.1:n.885-365_885-364delinsAG
XR_947273.1:n.448+8509_448+8510delinsAG
XR_947274.1:n.453-365_453-364delinsAG
XM_005270520.2:c.1579_1580delinsCT (CFAP57)	XP_005270577.1:p.Leu527=
XM_011540795.3:c.1579_1580delinsCT (CFAP57)	XP_011539097.1:p.Leu527=
XM_011540797.2:c.1516_1517delinsCT (CFAP57)	XP_011539099.1:p.Leu506=
XM_011540800.2:c.1579_1580delinsCT (CFAP57)	XP_011539102.1:p.Leu527=
XM_017000421.1:c.1579_1580delinsCT (CFAP57)	XP_016855910.1:p.Leu527=
XM_017000422.2:c.1579_1580delinsCT (CFAP57)	XP_016855911.1:p.Leu527=
XR_001736994.2:n.1708_1709delinsCT (CFAP57)
XR_001738021.1:n.532-365_532-364delinsAG
XR_001738022.1:n.529-365_529-364delinsAG
XR_001738023.2:n.827-365_827-364delinsAG
XR_001738024.1:n.539+8509_539+8510delinsAG
XR_947266.2:n.521-365_521-364delinsAG
XR_947268.2:n.247-365_247-364delinsAG
XR_947271.2:n.888-365_888-364delinsAG
XR_947273.2:n.538+8509_538+8510delinsAG
XR_947274.2:n.827-365_827-364delinsAG
NM_001195831.3:c.1579_1580delinsCT (CFAP57)	NP_001182760.2:p.Leu527=
NM_001378189.1:c.1579_1580delinsCT (CFAP57) MANE Select	NP_001365118.1:p.Leu527=