Canonical Allele Identifier: CA2741144307

Gene: CDKN1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2884989_2885012del , CM000673.2:g.2884989_2885012del	GRCh38
NC_000011.9:g.2906219_2906242del , CM000673.1:g.2906219_2906242del	GRCh37
NC_000011.8:g.2862795_2862818del	NCBI36
NG_008022.1:g.5758_5781del , LRG_533:g.5758_5781del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681969.1:n.142+626_142+649del
ENST00000380725.2:c.255+194_255+217del	ENSP00000370101.1:n.255+194_255+217del
ENST00000414822.8:c.482_505del	ENSP00000413720.3:p.Ala161_Pro168del
ENST00000430149.3:c.482_505del	ENSP00000411552.2:p.Ala161_Pro168del
ENST00000440480.8:c.449_472del MANE Select	ENSP00000411257.2:p.Ala150_Pro157del
ENST00000647251.1:c.255+194_255+217del	ENSP00000496631.1:n.255+194_255+217del
ENST00000380725.1:c.255+194_255+217del	ENSP00000370101.1:n.255+194_255+217del
ENST00000414822.7:c.482_505del	ENSP00000413720.3:p.Ala161_Pro168del
ENST00000430149.2:c.482_505del	ENSP00000411552.2:p.Ala161_Pro168del
ENST00000440480.6:c.449_472del	ENSP00000411257.2:p.Ala150_Pro157del
NM_000076.2:c.482_505del , LRG_533t1:c.482_505del	NP_000067.1:p.Ala161_Pro168del
NM_001122630.1:c.449_472del	NP_001116102.1:p.Ala150_Pro157del
NM_001122631.1:c.449_472del	NP_001116103.1:p.Ala150_Pro157del
XM_005252732.3:c.255+194_255+217del	XP_005252789.1:n.255+194_255+217del
NM_001362474.1:c.482_505del	NP_001349403.1:p.Ala161_Pro168del
NM_001362475.1:c.255+194_255+217del	NP_001349404.1:n.255+194_255+217del
NM_001122630.2:c.449_472del MANE Select	NP_001116102.1:p.Ala150_Pro157del
NM_001122631.2:c.449_472del	NP_001116103.1:p.Ala150_Pro157del
NM_001362474.2:c.482_505del	NP_001349403.1:p.Ala161_Pro168del
NM_001362475.2:c.255+194_255+217del	NP_001349404.1:n.255+194_255+217del