Canonical Allele Identifier: CA731281057

Gene: CENPF

Linked Data

• dbSNP Id: rs1169116047
• gnomAD v4: 1-214657482-CAA-C
• MyVariant Identifiers: chr1:g.214830826_214830827del (hg19) ; chr1:g.214657483_214657484del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657485_214657486del , CM000663.2:g.214657485_214657486del	GRCh38
NC_000001.10:g.214830828_214830829del , CM000663.1:g.214830828_214830829del	GRCh37
NC_000001.9:g.212897451_212897452del	NCBI36
NG_046787.1:g.59307_59308del

Transcript Alleles

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