Canonical Allele Identifier: CA1948368533
Gene: CDKN1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2884965_2884989delinsGACCGCGACCGGAGCCGCGACCGGA , CM000673.2:g.2884965_2884989delinsGACCGCGACCGGAGCCGCGACCGGA GRCh38
NC_000011.9:g.2906195_2906219delinsGACCGCGACCGGAGCCGCGACCGGA , CM000673.1:g.2906195_2906219delinsGACCGCGACCGGAGCCGCGACCGGA GRCh37
NC_000011.8:g.2862771_2862795delinsGACCGCGACCGGAGCCGCGACCGGA NCBI36
NG_008022.1:g.5777_5801delinsTCCGGTCGCGGCTCCGGTCGCGGTC , LRG_533:g.5777_5801delinsTCCGGTCGCGGCTCCGGTCGCGGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000681969.1:n.142+645_142+669delinsTCCGGTCGCGGCTCCGGTCGCGGTC
ENST00000380725.2:c.255+213_255+237delinsTCCGGTCGCGGCTCCGGTCGCGGTC ENSP00000370101.1:n.255+213_255+237delinsTCCGGTCGCGGCTCCGGTCG...
ENST00000414822.8:c.501_525delinsTCCGGTCGCGGCTCCGGTCGCGGTC ENSP00000413720.3:p.Ala167=
ENST00000430149.3:c.501_525delinsTCCGGTCGCGGCTCCGGTCGCGGTC ENSP00000411552.2:p.Ala167=
ENST00000440480.8:c.468_492delinsTCCGGTCGCGGCTCCGGTCGCGGTC MANE Select ENSP00000411257.2:p.Ala156=
ENST00000647251.1:c.255+213_255+237delinsTCCGGTCGCGGCTCCGGTCGCGGTC ENSP00000496631.1:n.255+213_255+237delinsTCCGGTCGCGGCTCCGGTCG...
ENST00000380725.1:c.255+213_255+237delinsTCCGGTCGCGGCTCCGGTCGCGGTC ENSP00000370101.1:n.255+213_255+237delinsTCCGGTCGCGGCTCCGGTCG...
ENST00000414822.7:c.501_525delinsTCCGGTCGCGGCTCCGGTCGCGGTC ENSP00000413720.3:p.Ala167=
ENST00000430149.2:c.501_525delinsTCCGGTCGCGGCTCCGGTCGCGGTC ENSP00000411552.2:p.Ala167=
ENST00000440480.6:c.468_492delinsTCCGGTCGCGGCTCCGGTCGCGGTC ENSP00000411257.2:p.Ala156=
NM_000076.2:c.501_525delinsTCCGGTCGCGGCTCCGGTCGCGGTC , LRG_533t1:c.501_525delinsTCCGGTCGCGGCTCCGGTCGCGGTC NP_000067.1:p.Ala167=
NM_001122630.1:c.468_492delinsTCCGGTCGCGGCTCCGGTCGCGGTC NP_001116102.1:p.Ala156=
NM_001122631.1:c.468_492delinsTCCGGTCGCGGCTCCGGTCGCGGTC NP_001116103.1:p.Ala156=
XM_005252732.3:c.255+213_255+237delinsTCCGGTCGCGGCTCCGGTCGCGGTC XP_005252789.1:n.255+213_255+237delinsTCCGGTCGCGGCTCCGGTCGCGG...
NM_001362474.1:c.501_525delinsTCCGGTCGCGGCTCCGGTCGCGGTC NP_001349403.1:p.Ala167=
NM_001362475.1:c.255+213_255+237delinsTCCGGTCGCGGCTCCGGTCGCGGTC NP_001349404.1:n.255+213_255+237delinsTCCGGTCGCGGCTCCGGTCGCGG...
NM_001122630.2:c.468_492delinsTCCGGTCGCGGCTCCGGTCGCGGTC MANE Select NP_001116102.1:p.Ala156=
NM_001122631.2:c.468_492delinsTCCGGTCGCGGCTCCGGTCGCGGTC NP_001116103.1:p.Ala156=
NM_001362474.2:c.501_525delinsTCCGGTCGCGGCTCCGGTCGCGGTC NP_001349403.1:p.Ala167=
NM_001362475.2:c.255+213_255+237delinsTCCGGTCGCGGCTCCGGTCGCGGTC NP_001349404.1:n.255+213_255+237delinsTCCGGTCGCGGCTCCGGTCGCGG...