Canonical Allele Identifier: CA344857916

Gene: CENPF

Linked Data

• gnomAD v4: 1-214657410-G-T
• MyVariant Identifiers: chr1:g.214830753G>T (hg19) ; chr1:g.214657410G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657410G>T , CM000663.2:g.214657410G>T	GRCh38
NC_000001.10:g.214830753G>T , CM000663.1:g.214830753G>T	GRCh37
NC_000001.9:g.212897376G>T	NCBI36
NG_046787.1:g.59232G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+1G>T	ENSP00000516538.1:n.8785+1G>T
ENST00000706766.1:n.1061+1G>T
ENST00000366955.8:c.8962+1G>T MANE Select	ENSP00000355922.3:n.8962+1G>T
ENST00000366955.7:c.8962+1G>T	ENSP00000355922.3:n.8962+1G>T
ENST00000469862.1:n.734G>T
NM_016343.3:c.8962+1G>T	NP_057427.3:n.8962+1G>T
XM_011509082.1:c.8785+1G>T	XP_011507384.1:n.8785+1G>T
XM_011509083.1:c.7897+1G>T	XP_011507385.1:n.7897+1G>T
XM_011509082.3:c.8785+1G>T	XP_011507384.1:n.8785+1G>T
XM_017000086.2:c.8962+1G>T	XP_016855575.1:n.8962+1G>T
NM_016343.4:c.8962+1G>T MANE Select	NP_057427.3:n.8962+1G>T