Canonical Allele Identifier: CA1948368454

Gene: CDKN1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2884893_2884911delinsGGCCGGGGCCGCGACTGGA , CM000673.2:g.2884893_2884911delinsGGCCGGGGCCGCGACTGGA	GRCh38
NC_000011.9:g.2906123_2906141delinsGGCCGGGGCCGCGACTGGA , CM000673.1:g.2906123_2906141delinsGGCCGGGGCCGCGACTGGA	GRCh37
NC_000011.8:g.2862699_2862717delinsGGCCGGGGCCGCGACTGGA	NCBI36
NG_008022.1:g.5855_5873delinsTCCAGTCGCGGCCCCGGCC , LRG_533:g.5855_5873delinsTCCAGTCGCGGCCCCGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681969.1:n.142+723_142+741delinsTCCAGTCGCGGCCCCGGCC
ENST00000380725.2:c.255+291_255+309delinsTCCAGTCGCGGCCCCGGCC	ENSP00000370101.1:n.255+291_255+309delinsTCCAGTCGCGGCCCCGGCC
ENST00000414822.8:c.579_597delinsTCCAGTCGCGGCCCCGGCC	ENSP00000413720.3:p.Ala193=
ENST00000430149.3:c.579_597delinsTCCAGTCGCGGCCCCGGCC	ENSP00000411552.2:p.Ala193=
ENST00000440480.8:c.546_564delinsTCCAGTCGCGGCCCCGGCC MANE Select	ENSP00000411257.2:p.Ala182=
ENST00000647251.1:c.255+291_255+309delinsTCCAGTCGCGGCCCCGGCC	ENSP00000496631.1:n.255+291_255+309delinsTCCAGTCGCGGCCCCGGCC
ENST00000380725.1:c.255+291_255+309delinsTCCAGTCGCGGCCCCGGCC	ENSP00000370101.1:n.255+291_255+309delinsTCCAGTCGCGGCCCCGGCC
ENST00000414822.7:c.579_597delinsTCCAGTCGCGGCCCCGGCC	ENSP00000413720.3:p.Ala193=
ENST00000430149.2:c.579_597delinsTCCAGTCGCGGCCCCGGCC	ENSP00000411552.2:p.Ala193=
ENST00000440480.6:c.546_564delinsTCCAGTCGCGGCCCCGGCC	ENSP00000411257.2:p.Ala182=
NM_000076.2:c.579_597delinsTCCAGTCGCGGCCCCGGCC , LRG_533t1:c.579_597delinsTCCAGTCGCGGCCCCGGCC	NP_000067.1:p.Ala193=
NM_001122630.1:c.546_564delinsTCCAGTCGCGGCCCCGGCC	NP_001116102.1:p.Ala182=
NM_001122631.1:c.546_564delinsTCCAGTCGCGGCCCCGGCC	NP_001116103.1:p.Ala182=
XM_005252732.3:c.255+291_255+309delinsTCCAGTCGCGGCCCCGGCC	XP_005252789.1:n.255+291_255+309delinsTCCAGTCGCGGCCCCGGCC
NM_001362474.1:c.579_597delinsTCCAGTCGCGGCCCCGGCC	NP_001349403.1:p.Ala193=
NM_001362475.1:c.255+291_255+309delinsTCCAGTCGCGGCCCCGGCC	NP_001349404.1:n.255+291_255+309delinsTCCAGTCGCGGCCCCGGCC
NM_001122630.2:c.546_564delinsTCCAGTCGCGGCCCCGGCC MANE Select	NP_001116102.1:p.Ala182=
NM_001122631.2:c.546_564delinsTCCAGTCGCGGCCCCGGCC	NP_001116103.1:p.Ala182=
NM_001362474.2:c.579_597delinsTCCAGTCGCGGCCCCGGCC	NP_001349403.1:p.Ala193=
NM_001362475.2:c.255+291_255+309delinsTCCAGTCGCGGCCCCGGCC	NP_001349404.1:n.255+291_255+309delinsTCCAGTCGCGGCCCCGGCC