Canonical Allele Identifier: CA529001873

Gene: CENPF

Linked Data

• dbSNP Id: rs1159497386
• gnomAD v2: 1-214830816-A-AT
• gnomAD v3: 1-214657473-A-AT
• gnomAD v4: 1-214657473-A-AT
• MyVariant Identifiers: chr1:g.214830816_214830817insT (hg19) ; chr1:g.214657473_214657474insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657474dup , CM000663.2:g.214657474dup	GRCh38
NC_000001.10:g.214830817dup , CM000663.1:g.214830817dup	GRCh37
NC_000001.9:g.212897440dup	NCBI36
NG_046787.1:g.59296dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+65dup	ENSP00000516538.1:n.8785+65dup
ENST00000706766.1:n.1061+65dup
ENST00000366955.8:c.8962+65dup MANE Select	ENSP00000355922.3:n.8962+65dup
ENST00000366955.7:c.8962+65dup	ENSP00000355922.3:n.8962+65dup
NM_016343.3:c.8962+65dup	NP_057427.3:n.8962+65dup
XM_011509082.1:c.8785+65dup	XP_011507384.1:n.8785+65dup
XM_011509083.1:c.7897+65dup	XP_011507385.1:n.7897+65dup
XM_011509082.3:c.8785+65dup	XP_011507384.1:n.8785+65dup
XM_017000086.2:c.8962+65dup	XP_016855575.1:n.8962+65dup
NM_016343.4:c.8962+65dup MANE Select	NP_057427.3:n.8962+65dup