Canonical Allele Identifier: CA2486377766

Gene: CENPF

Linked Data

• dbSNP Id: rs1169116047

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657485_214657486dup , CM000663.2:g.214657485_214657486dup	GRCh38
NC_000001.10:g.214830828_214830829dup , CM000663.1:g.214830828_214830829dup	GRCh37
NC_000001.9:g.212897451_212897452dup	NCBI36
NG_046787.1:g.59307_59308dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+76_8785+77dup	ENSP00000516538.1:n.8785+76_8785+77dup
ENST00000706766.1:n.1061+76_1061+77dup
ENST00000366955.8:c.8962+76_8962+77dup MANE Select	ENSP00000355922.3:n.8962+76_8962+77dup
ENST00000366955.7:c.8962+76_8962+77dup	ENSP00000355922.3:n.8962+76_8962+77dup
NM_016343.3:c.8962+76_8962+77dup	NP_057427.3:n.8962+76_8962+77dup
XM_011509082.1:c.8785+76_8785+77dup	XP_011507384.1:n.8785+76_8785+77dup
XM_011509083.1:c.7897+76_7897+77dup	XP_011507385.1:n.7897+76_7897+77dup
XM_011509082.3:c.8785+76_8785+77dup	XP_011507384.1:n.8785+76_8785+77dup
XM_017000086.2:c.8962+76_8962+77dup	XP_016855575.1:n.8962+76_8962+77dup
NM_016343.4:c.8962+76_8962+77dup MANE Select	NP_057427.3:n.8962+76_8962+77dup