Canonical Allele Identifier: CA2650488312

Gene: CENPF

Linked Data

• gnomAD v4: 1-214657485-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657486_214657487del , CM000663.2:g.214657486_214657487del	GRCh38
NC_000001.10:g.214830829_214830830del , CM000663.1:g.214830829_214830830del	GRCh37
NC_000001.9:g.212897452_212897453del	NCBI36
NG_046787.1:g.59308_59309del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+77_8785+78del	ENSP00000516538.1:n.8785+77_8785+78del
ENST00000706766.1:n.1061+77_1061+78del
ENST00000366955.8:c.8962+77_8962+78del MANE Select	ENSP00000355922.3:n.8962+77_8962+78del
ENST00000366955.7:c.8962+77_8962+78del	ENSP00000355922.3:n.8962+77_8962+78del
NM_016343.3:c.8962+77_8962+78del	NP_057427.3:n.8962+77_8962+78del
XM_011509082.1:c.8785+77_8785+78del	XP_011507384.1:n.8785+77_8785+78del
XM_011509083.1:c.7897+77_7897+78del	XP_011507385.1:n.7897+77_7897+78del
XM_011509082.3:c.8785+77_8785+78del	XP_011507384.1:n.8785+77_8785+78del
XM_017000086.2:c.8962+77_8962+78del	XP_016855575.1:n.8962+77_8962+78del
NM_016343.4:c.8962+77_8962+78del MANE Select	NP_057427.3:n.8962+77_8962+78del