Canonical Allele Identifier: CA344856867

Gene: CENPF

Linked Data

• gnomAD v4: 1-214657106-C-T
• MyVariant Identifiers: chr1:g.214830449C>T (hg19) ; chr1:g.214657106C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657106C>T , CM000663.2:g.214657106C>T	GRCh38
NC_000001.10:g.214830449C>T , CM000663.1:g.214830449C>T	GRCh37
NC_000001.9:g.212897072C>T	NCBI36
NG_046787.1:g.58928C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8482C>T	ENSP00000516538.1:p.His2828Tyr
ENST00000706766.1:n.758C>T
ENST00000366955.8:c.8659C>T MANE Select	ENSP00000355922.3:p.His2887Tyr
ENST00000366955.7:c.8659C>T	ENSP00000355922.3:p.His2887Tyr
ENST00000469862.1:n.430C>T
NM_016343.3:c.8659C>T	NP_057427.3:p.His2887Tyr
XM_011509082.1:c.8482C>T	XP_011507384.1:p.His2828Tyr
XM_011509083.1:c.7594C>T	XP_011507385.1:p.His2532Tyr
XM_011509082.3:c.8482C>T	XP_011507384.1:p.His2828Tyr
XM_017000086.2:c.8659C>T	XP_016855575.1:p.His2887Tyr
NM_016343.4:c.8659C>T MANE Select	NP_057427.3:p.His2887Tyr