Canonical Allele Identifier: CA916084226

Gene: CDKN1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2884857_2884858insCGGTGC , CM000673.2:g.2884857_2884858insCGGTGC	GRCh38
NC_000011.9:g.2906087_2906088insCGGTGC , CM000673.1:g.2906087_2906088insCGGTGC	GRCh37
NC_000011.8:g.2862663_2862664insCGGTGC	NCBI36
NG_008022.1:g.5908_5909insGCACCG , LRG_533:g.5908_5909insGCACCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681969.1:n.143-724_143-723insGCACCG
ENST00000380725.2:c.255+344_255+345insGCACCG	ENSP00000370101.1:n.255+344_255+345insGCACCG
ENST00000414822.8:c.632_633insGCACCG	ENSP00000413720.3:p.Ala211_Pro212insHisArg
ENST00000430149.3:c.632_633insGCACCG	ENSP00000411552.2:p.Ala211_Pro212insHisArg
ENST00000440480.8:c.599_600insGCACCG MANE Select	ENSP00000411257.2:p.Ala200_Pro201insHisArg
ENST00000647251.1:c.255+344_255+345insGCACCG	ENSP00000496631.1:n.255+344_255+345insGCACCG
ENST00000380725.1:c.255+344_255+345insGCACCG	ENSP00000370101.1:n.255+344_255+345insGCACCG
ENST00000414822.7:c.632_633insGCACCG	ENSP00000413720.3:p.Ala211_Pro212insHisArg
ENST00000430149.2:c.632_633insGCACCG	ENSP00000411552.2:p.Ala211_Pro212insHisArg
ENST00000440480.6:c.599_600insGCACCG	ENSP00000411257.2:p.Ala200_Pro201insHisArg
NM_000076.2:c.632_633insGCACCG , LRG_533t1:c.632_633insGCACCG	NP_000067.1:p.Ala211_Pro212insHisArg
NM_001122630.1:c.599_600insGCACCG	NP_001116102.1:p.Ala200_Pro201insHisArg
NM_001122631.1:c.599_600insGCACCG	NP_001116103.1:p.Ala200_Pro201insHisArg
XM_005252732.3:c.255+344_255+345insGCACCG	XP_005252789.1:n.255+344_255+345insGCACCG
NM_001362474.1:c.632_633insGCACCG	NP_001349403.1:p.Ala211_Pro212insHisArg
NM_001362475.1:c.255+344_255+345insGCACCG	NP_001349404.1:n.255+344_255+345insGCACCG
NM_001122630.2:c.599_600insGCACCG MANE Select	NP_001116102.1:p.Ala200_Pro201insHisArg
NM_001122631.2:c.599_600insGCACCG	NP_001116103.1:p.Ala200_Pro201insHisArg
NM_001362474.2:c.632_633insGCACCG	NP_001349403.1:p.Ala211_Pro212insHisArg
NM_001362475.2:c.255+344_255+345insGCACCG	NP_001349404.1:n.255+344_255+345insGCACCG