Canonical Allele Identifier: CA1948368449
Gene: CDKN1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2884890_2884938delinsTGGGGCCGGGGCCGCGACTGGAGCCGGGGCCGGAGCCGGAGCCGGAGCC , CM000673.2:g.2884890_2884938delinsTGGGGCCGGGGCCGCGACTGGAGCCGGGGCCGGAGCCGGAGCCGGAGCC GRCh38
NC_000011.9:g.2906120_2906168delinsTGGGGCCGGGGCCGCGACTGGAGCCGGGGCCGGAGCCGGAGCCGGAGCC , CM000673.1:g.2906120_2906168delinsTGGGGCCGGGGCCGCGACTGGAGCCGGGGCCGGAGCCGGAGCCGGAGCC GRCh37
NC_000011.8:g.2862696_2862744delinsTGGGGCCGGGGCCGCGACTGGAGCCGGGGCCGGAGCCGGAGCCGGAGCC NCBI36
NG_008022.1:g.5828_5876delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA , LRG_533:g.5828_5876delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000681969.1:n.142+696_142+744delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA
ENST00000380725.2:c.255+264_255+312delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA ENSP00000370101.1:n.255+264_255+312delinsGGCTCCGGCTCCGGCTCCGG...
ENST00000414822.8:c.552_600delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA ENSP00000413720.3:p.Pro184=
ENST00000430149.3:c.552_600delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA ENSP00000411552.2:p.Pro184=
ENST00000440480.8:c.519_567delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA MANE Select ENSP00000411257.2:p.Pro173=
ENST00000647251.1:c.255+264_255+312delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA ENSP00000496631.1:n.255+264_255+312delinsGGCTCCGGCTCCGGCTCCGG...
ENST00000380725.1:c.255+264_255+312delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA ENSP00000370101.1:n.255+264_255+312delinsGGCTCCGGCTCCGGCTCCGG...
ENST00000414822.7:c.552_600delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA ENSP00000413720.3:p.Pro184=
ENST00000430149.2:c.552_600delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA ENSP00000411552.2:p.Pro184=
ENST00000440480.6:c.519_567delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA ENSP00000411257.2:p.Pro173=
NM_000076.2:c.552_600delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA , LRG_533t1:c.552_600delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA NP_000067.1:p.Pro184=
NM_001122630.1:c.519_567delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA NP_001116102.1:p.Pro173=
NM_001122631.1:c.519_567delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA NP_001116103.1:p.Pro173=
XM_005252732.3:c.255+264_255+312delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA XP_005252789.1:n.255+264_255+312delinsGGCTCCGGCTCCGGCTCCGGCCC...
NM_001362474.1:c.552_600delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA NP_001349403.1:p.Pro184=
NM_001362475.1:c.255+264_255+312delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA NP_001349404.1:n.255+264_255+312delinsGGCTCCGGCTCCGGCTCCGGCCC...
NM_001122630.2:c.519_567delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA MANE Select NP_001116102.1:p.Pro173=
NM_001122631.2:c.519_567delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA NP_001116103.1:p.Pro173=
NM_001362474.2:c.552_600delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA NP_001349403.1:p.Pro184=
NM_001362475.2:c.255+264_255+312delinsGGCTCCGGCTCCGGCTCCGGCCCCGGCTCCAGTCGCGGCCCCGGCCCCA NP_001349404.1:n.255+264_255+312delinsGGCTCCGGCTCCGGCTCCGGCCC...