Canonical Allele Identifier: CA2497029247
Gene: CDKN1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2884966_2884978delinsACCGCGACCGGAG , CM000673.2:g.2884966_2884978delinsACCGCGACCGGAG GRCh38
NC_000011.9:g.2906196_2906208delinsACCGCGACCGGAG , CM000673.1:g.2906196_2906208delinsACCGCGACCGGAG GRCh37
NC_000011.8:g.2862772_2862784delinsACCGCGACCGGAG NCBI36
NG_008022.1:g.5788_5800delinsCTCCGGTCGCGGT , LRG_533:g.5788_5800delinsCTCCGGTCGCGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000681969.1:n.142+656_142+668delinsCTCCGGTCGCGGT
ENST00000380725.2:c.255+224_255+236delinsCTCCGGTCGCGGT ENSP00000370101.1:n.255+224_255+236delinsCTCCGGTCGCGGT
ENST00000414822.8:c.512_524delinsCTCCGGTCGCGGT ENSP00000413720.3:p.Ala171=
ENST00000430149.3:c.512_524delinsCTCCGGTCGCGGT ENSP00000411552.2:p.Ala171=
ENST00000440480.8:c.479_491delinsCTCCGGTCGCGGT MANE Select ENSP00000411257.2:p.Ala160=
ENST00000647251.1:c.255+224_255+236delinsCTCCGGTCGCGGT ENSP00000496631.1:n.255+224_255+236delinsCTCCGGTCGCGGT
ENST00000380725.1:c.255+224_255+236delinsCTCCGGTCGCGGT ENSP00000370101.1:n.255+224_255+236delinsCTCCGGTCGCGGT
ENST00000414822.7:c.512_524delinsCTCCGGTCGCGGT ENSP00000413720.3:p.Ala171=
ENST00000430149.2:c.512_524delinsCTCCGGTCGCGGT ENSP00000411552.2:p.Ala171=
ENST00000440480.6:c.479_491delinsCTCCGGTCGCGGT ENSP00000411257.2:p.Ala160=
NM_000076.2:c.512_524delinsCTCCGGTCGCGGT , LRG_533t1:c.512_524delinsCTCCGGTCGCGGT NP_000067.1:p.Ala171=
NM_001122630.1:c.479_491delinsCTCCGGTCGCGGT NP_001116102.1:p.Ala160=
NM_001122631.1:c.479_491delinsCTCCGGTCGCGGT NP_001116103.1:p.Ala160=
XM_005252732.3:c.255+224_255+236delinsCTCCGGTCGCGGT XP_005252789.1:n.255+224_255+236delinsCTCCGGTCGCGGT
NM_001362474.1:c.512_524delinsCTCCGGTCGCGGT NP_001349403.1:p.Ala171=
NM_001362475.1:c.255+224_255+236delinsCTCCGGTCGCGGT NP_001349404.1:n.255+224_255+236delinsCTCCGGTCGCGGT
NM_001122630.2:c.479_491delinsCTCCGGTCGCGGT MANE Select NP_001116102.1:p.Ala160=
NM_001122631.2:c.479_491delinsCTCCGGTCGCGGT NP_001116103.1:p.Ala160=
NM_001362474.2:c.512_524delinsCTCCGGTCGCGGT NP_001349403.1:p.Ala171=
NM_001362475.2:c.255+224_255+236delinsCTCCGGTCGCGGT NP_001349404.1:n.255+224_255+236delinsCTCCGGTCGCGGT