Canonical Allele Identifier: CA37381001

Gene: CENPF

Linked Data

• dbSNP Id: rs890140820
• gnomAD v2: 1-214830419-G-A
• gnomAD v4: 1-214657076-G-A
• MyVariant Identifiers: chr1:g.214830419G>A (hg19) ; chr1:g.214657076G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657076G>A , CM000663.2:g.214657076G>A	GRCh38
NC_000001.10:g.214830419G>A , CM000663.1:g.214830419G>A	GRCh37
NC_000001.9:g.212897042G>A	NCBI36
NG_046787.1:g.58898G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000706765.1:c.8452G>A	ENSP00000516538.1:p.Ala2818Thr
ENST00000706766.1:n.728G>A
ENST00000366955.8:c.8629G>A MANE Select	ENSP00000355922.3:p.Ala2877Thr
ENST00000366955.7:c.8629G>A	ENSP00000355922.3:p.Ala2877Thr
ENST00000469862.1:n.400G>A
NM_016343.3:c.8629G>A	NP_057427.3:p.Ala2877Thr
XM_011509082.1:c.8452G>A	XP_011507384.1:p.Ala2818Thr
XM_011509083.1:c.7564G>A	XP_011507385.1:p.Ala2522Thr
XM_011509082.3:c.8452G>A	XP_011507384.1:p.Ala2818Thr
XM_017000086.2:c.8629G>A	XP_016855575.1:p.Ala2877Thr
NM_016343.4:c.8629G>A MANE Select	NP_057427.3:p.Ala2877Thr