Canonical Allele Identifier: CA970769

Gene: CDC14A

Linked Data

• ClinVar Variation Id: 235146
• ClinVar RCV Id: RCV000223953 ; RCV002259325
• dbSNP Id: rs777112652
• ExAC: 1:100949885 C / T
• gnomAD v2: 1-100949885-C-T
• gnomAD v3: 1-100484329-C-T
• gnomAD v4: 1-100484329-C-T
• MyVariant Identifiers: chr1:g.100949885C>T (hg19) ; chr1:g.100484329C>T (hg38)
• PubMed: PMID:27259055

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100484329C>T , CM000663.2:g.100484329C>T	GRCh38
NC_000001.10:g.100949885C>T , CM000663.1:g.100949885C>T	GRCh37
NC_000001.9:g.100722473C>T	NCBI36
NG_051602.1:g.144315C>T
NG_051602.2:g.144329C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336454.5:c.1015C>T MANE Select	ENSP00000336739.3:p.Arg339Ter
ENST00000361544.11:c.1015C>T	ENSP00000354916.6:p.Arg339Ter
ENST00000370124.8:c.1015C>T	ENSP00000359142.3:p.Arg339Ter
ENST00000635056.2:c.841C>T	ENSP00000489217.1:p.Arg281Ter
ENST00000644676.1:c.1018C>T	ENSP00000494661.1:p.Arg340Ter
ENST00000644813.1:c.1015C>T	ENSP00000496374.1:p.Arg339Ter
ENST00000644844.1:c.841C>T	ENSP00000494417.1:p.Arg281Ter
ENST00000646563.1:c.*351C>T	ENSP00000493651.1:n.*351C>T
ENST00000646665.1:c.*664C>T	ENSP00000496153.1:n.*664C>T
ENST00000647005.1:c.841C>T	ENSP00000495617.1:p.Arg281Ter
ENST00000647203.1:c.974C>T	ENSP00000494551.1:p.Pro325Leu
ENST00000336454.3:c.1015C>T	ENSP00000336739.3:p.Arg339Ter
ENST00000361544.10:c.1015C>T	ENSP00000354916.6:p.Arg339Ter
ENST00000370124.7:c.1015C>T	ENSP00000359142.3:p.Arg339Ter
ENST00000635056.1:c.841C>T	ENSP00000489217.1:p.Arg281Ter
NM_003672.3:c.1015C>T	NP_003663.2:p.Arg339Ter
NM_033312.2:c.1015C>T	NP_201569.1:p.Arg339Ter
NM_033313.2:c.1015C>T	NP_201570.1:p.Arg339Ter
XM_005271294.2:c.1018C>T	XP_005271351.1:p.Arg340Ter
XM_005271296.2:c.1018C>T	XP_005271353.1:p.Arg340Ter
XM_011542340.1:c.1018C>T	XP_011540642.1:p.Arg340Ter
XM_011542341.1:c.979C>T	XP_011540643.1:p.Arg327Ter
XM_011542342.1:c.1015C>T	XP_011540644.1:p.Arg339Ter
XM_011542343.1:c.880C>T	XP_011540645.1:p.Arg294Ter
XM_011542344.1:c.841C>T	XP_011540646.1:p.Arg281Ter
XM_011542345.1:c.631C>T	XP_011540647.1:p.Arg211Ter
XM_011542346.1:c.1018C>T	XP_011540648.1:p.Arg340Ter
NM_001319210.1:c.1015C>T	NP_001306139.1:p.Arg339Ter
NM_001319211.1:c.841C>T	NP_001306140.1:p.Arg281Ter
NM_001319212.1:c.136C>T	NP_001306141.1:p.Arg46Ter
XM_005271294.3:c.1018C>T	XP_005271351.1:p.Arg340Ter
XM_005271296.3:c.1018C>T	XP_005271353.1:p.Arg340Ter
XM_011542340.2:c.1018C>T	XP_011540642.1:p.Arg340Ter
XM_011542341.3:c.979C>T	XP_011540643.1:p.Arg327Ter
XM_011542345.3:c.631C>T	XP_011540647.1:p.Arg211Ter
XM_017002646.1:c.1018C>T	XP_016858135.1:p.Arg340Ter
XM_017002647.1:c.1015C>T	XP_016858136.1:p.Arg339Ter
XM_024450503.1:c.841C>T	XP_024306271.1:p.Arg281Ter
XM_024450504.1:c.136C>T	XP_024306272.1:p.Arg46Ter
XM_024450505.1:c.136C>T	XP_024306273.1:p.Arg46Ter
XM_024450506.1:c.136C>T	XP_024306274.1:p.Arg46Ter
XR_002957887.1:n.1051C>T
XR_002957888.1:n.1149C>T
NM_003672.4:c.1015C>T MANE Select	NP_003663.2:p.Arg339Ter
NM_001319210.2:c.1015C>T	NP_001306139.1:p.Arg339Ter
NM_001319211.2:c.841C>T	NP_001306140.1:p.Arg281Ter
NM_001319212.2:c.136C>T	NP_001306141.1:p.Arg46Ter
NM_033312.3:c.1015C>T	NP_201569.1:p.Arg339Ter
NM_033313.3:c.1015C>T	NP_201570.1:p.Arg339Ter