Canonical Allele Identifier: CA16613541
Gene: CDKN1C HGNC NCBI

Linked Data

ClinVar Variation Id: 412843
ClinVar RCV Id: RCV000457216
dbSNP Id: rs1064792990

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2884874_2884903del , CM000673.2:g.2884874_2884903del GRCh38
NC_000011.9:g.2906104_2906133del , CM000673.1:g.2906104_2906133del GRCh37
NC_000011.8:g.2862680_2862709del NCBI36
NG_008022.1:g.5876_5905del , LRG_533:g.5876_5905del

Transcript Alleles

HGVS Amino-acid Change
ENST00000681969.1:n.142+744_143-727del
ENST00000380725.2:c.255+312_255+341del ENSP00000370101.1:n.255+312_255+341del
ENST00000414822.8:c.600_629del ENSP00000413720.3:p.Ala201_Pro210del
ENST00000430149.3:c.600_629del ENSP00000411552.2:p.Ala201_Pro210del
ENST00000440480.8:c.567_596del MANE Select ENSP00000411257.2:p.Ala190_Pro199del
ENST00000647251.1:c.255+312_255+341del ENSP00000496631.1:n.255+312_255+341del
ENST00000380725.1:c.255+312_255+341del ENSP00000370101.1:n.255+312_255+341del
ENST00000414822.7:c.600_629del ENSP00000413720.3:p.Ala201_Pro210del
ENST00000430149.2:c.600_629del ENSP00000411552.2:p.Ala201_Pro210del
ENST00000440480.6:c.567_596del ENSP00000411257.2:p.Ala190_Pro199del
NM_000076.2:c.600_629del , LRG_533t1:c.600_629del NP_000067.1:p.Ala201_Pro210del
NM_001122630.1:c.567_596del NP_001116102.1:p.Ala190_Pro199del
NM_001122631.1:c.567_596del NP_001116103.1:p.Ala190_Pro199del
XM_005252732.3:c.255+312_255+341del XP_005252789.1:n.255+312_255+341del
NM_001362474.1:c.600_629del NP_001349403.1:p.Ala201_Pro210del
NM_001362475.1:c.255+312_255+341del NP_001349404.1:n.255+312_255+341del
NM_001122630.2:c.567_596del MANE Select NP_001116102.1:p.Ala190_Pro199del
NM_001122631.2:c.567_596del NP_001116103.1:p.Ala190_Pro199del
NM_001362474.2:c.600_629del NP_001349403.1:p.Ala201_Pro210del
NM_001362475.2:c.255+312_255+341del NP_001349404.1:n.255+312_255+341del