Canonical Allele Identifier: CA2486377726

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657408_214657409delinsAG , CM000663.2:g.214657408_214657409delinsAG	GRCh38
NC_000001.10:g.214830751_214830752delinsAG , CM000663.1:g.214830751_214830752delinsAG	GRCh37
NC_000001.9:g.212897374_212897375delinsAG	NCBI36
NG_046787.1:g.59230_59231delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8784_8785delinsAG	ENSP00000516538.1:p.Lys2928=
ENST00000706766.1:n.1060_1061delinsAG
ENST00000366955.8:c.8961_8962delinsAG MANE Select	ENSP00000355922.3:p.Lys2987=
ENST00000366955.7:c.8961_8962delinsAG	ENSP00000355922.3:p.Lys2987=
ENST00000469862.1:n.732_733delinsAG
NM_016343.3:c.8961_8962delinsAG	NP_057427.3:p.Lys2987=
XM_011509082.1:c.8784_8785delinsAG	XP_011507384.1:p.Lys2928=
XM_011509083.1:c.7896_7897delinsAG	XP_011507385.1:p.Lys2632=
XM_011509082.3:c.8784_8785delinsAG	XP_011507384.1:p.Lys2928=
XM_017000086.2:c.8961_8962delinsAG	XP_016855575.1:p.Lys2987=
NM_016343.4:c.8961_8962delinsAG MANE Select	NP_057427.3:p.Lys2987=