Canonical Allele Identifier: CA2486377767

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657483_214657496delinsAAAAGTATTTGCTT , CM000663.2:g.214657483_214657496delinsAAAAGTATTTGCTT	GRCh38
NC_000001.10:g.214830826_214830839delinsAAAAGTATTTGCTT , CM000663.1:g.214830826_214830839delinsAAAAGTATTTGCTT	GRCh37
NC_000001.9:g.212897449_212897462delinsAAAAGTATTTGCTT	NCBI36
NG_046787.1:g.59305_59318delinsAAAAGTATTTGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+74_8785+87delinsAAAAGTATTTGCTT	ENSP00000516538.1:n.8785+74_8785+87delinsAAAAGTATTTGCTT
ENST00000706766.1:n.1061+74_1061+87delinsAAAAGTATTTGCTT
ENST00000366955.8:c.8962+74_8962+87delinsAAAAGTATTTGCTT MANE Select	ENSP00000355922.3:n.8962+74_8962+87delinsAAAAGTATTTGCTT
ENST00000366955.7:c.8962+74_8962+87delinsAAAAGTATTTGCTT	ENSP00000355922.3:n.8962+74_8962+87delinsAAAAGTATTTGCTT
NM_016343.3:c.8962+74_8962+87delinsAAAAGTATTTGCTT	NP_057427.3:n.8962+74_8962+87delinsAAAAGTATTTGCTT
XM_011509082.1:c.8785+74_8785+87delinsAAAAGTATTTGCTT	XP_011507384.1:n.8785+74_8785+87delinsAAAAGTATTTGCTT
XM_011509083.1:c.7897+74_7897+87delinsAAAAGTATTTGCTT	XP_011507385.1:n.7897+74_7897+87delinsAAAAGTATTTGCTT
XM_011509082.3:c.8785+74_8785+87delinsAAAAGTATTTGCTT	XP_011507384.1:n.8785+74_8785+87delinsAAAAGTATTTGCTT
XM_017000086.2:c.8962+74_8962+87delinsAAAAGTATTTGCTT	XP_016855575.1:n.8962+74_8962+87delinsAAAAGTATTTGCTT
NM_016343.4:c.8962+74_8962+87delinsAAAAGTATTTGCTT MANE Select	NP_057427.3:n.8962+74_8962+87delinsAAAAGTATTTGCTT