Canonical Allele Identifier: CA1165524815

Gene: CFAP57 EBNA1BP2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43206672_43206676delinsTGTAA , CM000663.2:g.43206672_43206676delinsTGTAA	GRCh38
NC_000001.10:g.43672343_43672347delinsTGTAA , CM000663.1:g.43672343_43672347delinsTGTAA	GRCh37
NC_000001.9:g.43444930_43444934delinsTGTAA	NCBI36
NG_028079.1:g.39343_39347delinsTGTAA
NG_028079.2:g.39343_39347delinsTGTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372492.9:c.1543-48_1543-44delinsTGTAA (CFAP57) MANE Select	ENSP00000361570.4:n.1543-48_1543-44delinsTGTAA
ENST00000372492.8:c.1543-48_1543-44delinsTGTAA (CFAP57)	ENSP00000361570.4:n.1543-48_1543-44delinsTGTAA
ENST00000461557.2:n.233+4774_233+4778delinsTTACA (EBNA1BP2)
ENST00000466927.5:n.197+8590_197+8594delinsTTACA (EBNA1BP2)
ENST00000474566.1:n.420-284_420-280delinsTTACA (EBNA1BP2)
ENST00000528956.5:c.1543-48_1543-44delinsTGTAA (CFAP57)	ENSP00000435310.1:n.1543-48_1543-44delinsTGTAA
ENST00000533339.1:c.*1442-48_*1442-44delinsTGTAA (CFAP57)	ENSP00000432547.1:n.*1442-48_*1442-44delinsTGTAA
ENST00000610710.4:c.1543-48_1543-44delinsTGTAA (CFAP57)	ENSP00000479773.1:n.1543-48_1543-44delinsTGTAA
NM_001167965.1:c.1543-48_1543-44delinsTGTAA (CFAP57)	NP_001161437.1:n.1543-48_1543-44delinsTGTAA
NM_001195831.2:c.1543-48_1543-44delinsTGTAA (CFAP57)	NP_001182760.2:n.1543-48_1543-44delinsTGTAA
NM_152498.3:c.1543-48_1543-44delinsTGTAA (CFAP57)	NP_689711.2:n.1543-48_1543-44delinsTGTAA
XM_005270520.1:c.1543-48_1543-44delinsTGTAA (CFAP57)	XP_005270577.1:n.1543-48_1543-44delinsTGTAA
XM_006710383.1:c.1510-48_1510-44delinsTGTAA (CFAP57)	XP_006710446.1:n.1510-48_1510-44delinsTGTAA
XM_011540793.1:c.1543-48_1543-44delinsTGTAA (CFAP57)	XP_011539095.1:n.1543-48_1543-44delinsTGTAA
XM_011540794.1:c.1543-48_1543-44delinsTGTAA (CFAP57)	XP_011539096.1:n.1543-48_1543-44delinsTGTAA
XM_011540795.1:c.1543-48_1543-44delinsTGTAA (CFAP57)	XP_011539097.1:n.1543-48_1543-44delinsTGTAA
XM_011540796.1:c.1510-48_1510-44delinsTGTAA (CFAP57)	XP_011539098.1:n.1510-48_1510-44delinsTGTAA
XM_011540797.1:c.1480-48_1480-44delinsTGTAA (CFAP57)	XP_011539099.1:n.1480-48_1480-44delinsTGTAA
XM_011540798.1:c.1543-3071_1543-3067delinsTGTAA (CFAP57)	XP_011539100.1:n.1543-3071_1543-3067delinsTGTAA
XM_011540799.1:c.1542+7169_1542+7173delinsTGTAA (CFAP57)	XP_011539101.1:n.1542+7169_1542+7173delinsTGTAA
XM_011540800.1:c.1543-48_1543-44delinsTGTAA (CFAP57)	XP_011539102.1:n.1543-48_1543-44delinsTGTAA
XM_011540801.1:c.1543-48_1543-44delinsTGTAA (CFAP57)	XP_011539103.1:n.1543-48_1543-44delinsTGTAA
XR_947266.1:n.450-284_450-280delinsTTACA
XR_947267.1:n.455-284_455-280delinsTTACA
XR_947268.1:n.240-284_240-280delinsTTACA
XR_947269.1:n.1064-284_1064-280delinsTTACA
XR_947270.1:n.214-284_214-280delinsTTACA
XR_947271.1:n.885-284_885-280delinsTTACA
XR_947273.1:n.448+8590_448+8594delinsTTACA
XR_947274.1:n.453-284_453-280delinsTTACA
XM_005270520.2:c.1543-48_1543-44delinsTGTAA (CFAP57)	XP_005270577.1:n.1543-48_1543-44delinsTGTAA
XM_011540795.3:c.1543-48_1543-44delinsTGTAA (CFAP57)	XP_011539097.1:n.1543-48_1543-44delinsTGTAA
XM_011540797.2:c.1480-48_1480-44delinsTGTAA (CFAP57)	XP_011539099.1:n.1480-48_1480-44delinsTGTAA
XM_011540800.2:c.1543-48_1543-44delinsTGTAA (CFAP57)	XP_011539102.1:n.1543-48_1543-44delinsTGTAA
XM_017000421.1:c.1543-48_1543-44delinsTGTAA (CFAP57)	XP_016855910.1:n.1543-48_1543-44delinsTGTAA
XM_017000422.2:c.1543-48_1543-44delinsTGTAA (CFAP57)	XP_016855911.1:n.1543-48_1543-44delinsTGTAA
XR_001736994.2:n.1672-48_1672-44delinsTGTAA (CFAP57)
XR_001738021.1:n.532-284_532-280delinsTTACA
XR_001738022.1:n.529-284_529-280delinsTTACA
XR_001738023.2:n.827-284_827-280delinsTTACA
XR_001738024.1:n.539+8590_539+8594delinsTTACA
XR_947266.2:n.521-284_521-280delinsTTACA
XR_947268.2:n.247-284_247-280delinsTTACA
XR_947271.2:n.888-284_888-280delinsTTACA
XR_947273.2:n.538+8590_538+8594delinsTTACA
XR_947274.2:n.827-284_827-280delinsTTACA
NM_001195831.3:c.1543-48_1543-44delinsTGTAA (CFAP57)	NP_001182760.2:n.1543-48_1543-44delinsTGTAA
NM_001378189.1:c.1543-48_1543-44delinsTGTAA (CFAP57) MANE Select	NP_001365118.1:n.1543-48_1543-44delinsTGTAA