Canonical Allele Identifier: CA2486377765

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657482_214657484delinsCAA , CM000663.2:g.214657482_214657484delinsCAA	GRCh38
NC_000001.10:g.214830825_214830827delinsCAA , CM000663.1:g.214830825_214830827delinsCAA	GRCh37
NC_000001.9:g.212897448_212897450delinsCAA	NCBI36
NG_046787.1:g.59304_59306delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+73_8785+75delinsCAA	ENSP00000516538.1:n.8785+73_8785+75delinsCAA
ENST00000706766.1:n.1061+73_1061+75delinsCAA
ENST00000366955.8:c.8962+73_8962+75delinsCAA MANE Select	ENSP00000355922.3:n.8962+73_8962+75delinsCAA
ENST00000366955.7:c.8962+73_8962+75delinsCAA	ENSP00000355922.3:n.8962+73_8962+75delinsCAA
NM_016343.3:c.8962+73_8962+75delinsCAA	NP_057427.3:n.8962+73_8962+75delinsCAA
XM_011509082.1:c.8785+73_8785+75delinsCAA	XP_011507384.1:n.8785+73_8785+75delinsCAA
XM_011509083.1:c.7897+73_7897+75delinsCAA	XP_011507385.1:n.7897+73_7897+75delinsCAA
XM_011509082.3:c.8785+73_8785+75delinsCAA	XP_011507384.1:n.8785+73_8785+75delinsCAA
XM_017000086.2:c.8962+73_8962+75delinsCAA	XP_016855575.1:n.8962+73_8962+75delinsCAA
NM_016343.4:c.8962+73_8962+75delinsCAA MANE Select	NP_057427.3:n.8962+73_8962+75delinsCAA