Canonical Allele Identifier: CA1389885
Gene: CENPF HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid change
ENST00000706764.1:n.1111A>T
ENST00000706765.1:c.933A>T ENSP00000516538.1:p.Gln311His
ENST00000366955.8:c.933A>T MANE Select ENSP00000355922.3:p.Gln311His
ENST00000366955.7:c.933A>T ENSP00000355922.3:p.Gln311His
NM_016343.3:c.933A>T NP_057427.3:p.Gln311His
XM_011509082.1:c.933A>T XP_011507384.1:p.Gln311His
XM_011509082.3:c.933A>T XP_011507384.1:p.Gln311His
XM_017000086.2:c.933A>T XP_016855575.1:p.Gln311His
NM_016343.4:c.933A>T MANE Select NP_057427.3:p.Gln311His
Search 100 bp 5'
Search 100 bp 3'