Canonical Allele Identifier: CA1389884

Gene: CENPF

Linked Data

• dbSNP Id: rs146767943
• ExAC: 1:214795489 A / G
• gnomAD v2: 1-214795489-A-G
• gnomAD v3: 1-214622146-A-G
• gnomAD v4: 1-214622146-A-G
• MyVariant Identifiers: chr1:g.214795489A>G (hg19) ; chr1:g.214622146A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214622146A>G , CM000663.2:g.214622146A>G	GRCh38
NC_000001.10:g.214795489A>G , CM000663.1:g.214795489A>G	GRCh37
NC_000001.9:g.212862112A>G	NCBI36
NG_046787.1:g.23968A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706764.1:n.1111A>G
ENST00000706765.1:c.933A>G	ENSP00000516538.1:p.Gln311=
ENST00000366955.8:c.933A>G MANE Select	ENSP00000355922.3:p.Gln311=
ENST00000366955.7:c.933A>G	ENSP00000355922.3:p.Gln311=
NM_016343.3:c.933A>G	NP_057427.3:p.Gln311=
XM_011509082.1:c.933A>G	XP_011507384.1:p.Gln311=
XM_011509082.3:c.933A>G	XP_011507384.1:p.Gln311=
XM_017000086.2:c.933A>G	XP_016855575.1:p.Gln311=
NM_016343.4:c.933A>G MANE Select	NP_057427.3:p.Gln311=