Canonical Allele Identifier: CA1948368536
Gene: CDKN1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2884966_2884990delinsACCGCGACCGGAGCCGCGACCGGAG , CM000673.2:g.2884966_2884990delinsACCGCGACCGGAGCCGCGACCGGAG GRCh38
NC_000011.9:g.2906196_2906220delinsACCGCGACCGGAGCCGCGACCGGAG , CM000673.1:g.2906196_2906220delinsACCGCGACCGGAGCCGCGACCGGAG GRCh37
NC_000011.8:g.2862772_2862796delinsACCGCGACCGGAGCCGCGACCGGAG NCBI36
NG_008022.1:g.5776_5800delinsCTCCGGTCGCGGCTCCGGTCGCGGT , LRG_533:g.5776_5800delinsCTCCGGTCGCGGCTCCGGTCGCGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000681969.1:n.142+644_142+668delinsCTCCGGTCGCGGCTCCGGTCGCGGT
ENST00000380725.2:c.255+212_255+236delinsCTCCGGTCGCGGCTCCGGTCGCGGT ENSP00000370101.1:n.255+212_255+236delinsCTCCGGTCGCGGCTCCGGTC...
ENST00000414822.8:c.500_524delinsCTCCGGTCGCGGCTCCGGTCGCGGT ENSP00000413720.3:p.Ala167=
ENST00000430149.3:c.500_524delinsCTCCGGTCGCGGCTCCGGTCGCGGT ENSP00000411552.2:p.Ala167=
ENST00000440480.8:c.467_491delinsCTCCGGTCGCGGCTCCGGTCGCGGT MANE Select ENSP00000411257.2:p.Ala156=
ENST00000647251.1:c.255+212_255+236delinsCTCCGGTCGCGGCTCCGGTCGCGGT ENSP00000496631.1:n.255+212_255+236delinsCTCCGGTCGCGGCTCCGGTC...
ENST00000380725.1:c.255+212_255+236delinsCTCCGGTCGCGGCTCCGGTCGCGGT ENSP00000370101.1:n.255+212_255+236delinsCTCCGGTCGCGGCTCCGGTC...
ENST00000414822.7:c.500_524delinsCTCCGGTCGCGGCTCCGGTCGCGGT ENSP00000413720.3:p.Ala167=
ENST00000430149.2:c.500_524delinsCTCCGGTCGCGGCTCCGGTCGCGGT ENSP00000411552.2:p.Ala167=
ENST00000440480.6:c.467_491delinsCTCCGGTCGCGGCTCCGGTCGCGGT ENSP00000411257.2:p.Ala156=
NM_000076.2:c.500_524delinsCTCCGGTCGCGGCTCCGGTCGCGGT , LRG_533t1:c.500_524delinsCTCCGGTCGCGGCTCCGGTCGCGGT NP_000067.1:p.Ala167=
NM_001122630.1:c.467_491delinsCTCCGGTCGCGGCTCCGGTCGCGGT NP_001116102.1:p.Ala156=
NM_001122631.1:c.467_491delinsCTCCGGTCGCGGCTCCGGTCGCGGT NP_001116103.1:p.Ala156=
XM_005252732.3:c.255+212_255+236delinsCTCCGGTCGCGGCTCCGGTCGCGGT XP_005252789.1:n.255+212_255+236delinsCTCCGGTCGCGGCTCCGGTCGCG...
NM_001362474.1:c.500_524delinsCTCCGGTCGCGGCTCCGGTCGCGGT NP_001349403.1:p.Ala167=
NM_001362475.1:c.255+212_255+236delinsCTCCGGTCGCGGCTCCGGTCGCGGT NP_001349404.1:n.255+212_255+236delinsCTCCGGTCGCGGCTCCGGTCGCG...
NM_001122630.2:c.467_491delinsCTCCGGTCGCGGCTCCGGTCGCGGT MANE Select NP_001116102.1:p.Ala156=
NM_001122631.2:c.467_491delinsCTCCGGTCGCGGCTCCGGTCGCGGT NP_001116103.1:p.Ala156=
NM_001362474.2:c.500_524delinsCTCCGGTCGCGGCTCCGGTCGCGGT NP_001349403.1:p.Ala167=
NM_001362475.2:c.255+212_255+236delinsCTCCGGTCGCGGCTCCGGTCGCGGT NP_001349404.1:n.255+212_255+236delinsCTCCGGTCGCGGCTCCGGTCGCG...