Canonical Allele Identifier: CA1948368526

Gene: CDKN1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2884960A= , CM000673.2:g.2884960A=	GRCh38
NC_000011.9:g.2906190A= , CM000673.1:g.2906190A=	GRCh37
NC_000011.8:g.2862766A=	NCBI36
NG_008022.1:g.5806T= , LRG_533:g.5806T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681969.1:n.142+674T=
ENST00000380725.2:c.255+242T=	ENSP00000370101.1:n.255+242T=
ENST00000414822.8:c.530T=	ENSP00000413720.3:p.Val177=
ENST00000430149.3:c.530T=	ENSP00000411552.2:p.Val177=
ENST00000440480.8:c.497T= MANE Select	ENSP00000411257.2:p.Val166=
ENST00000647251.1:c.255+242T=	ENSP00000496631.1:n.255+242T=
ENST00000380725.1:c.255+242T=	ENSP00000370101.1:n.255+242T=
ENST00000414822.7:c.530T=	ENSP00000413720.3:p.Val177=
ENST00000430149.2:c.530T=	ENSP00000411552.2:p.Val177=
ENST00000440480.6:c.497T=	ENSP00000411257.2:p.Val166=
NM_000076.2:c.530T= , LRG_533t1:c.530T=	NP_000067.1:p.Val177=
NM_001122630.1:c.497T=	NP_001116102.1:p.Val166=
NM_001122631.1:c.497T=	NP_001116103.1:p.Val166=
XM_005252732.3:c.255+242T=	XP_005252789.1:n.255+242T=
NM_001362474.1:c.530T=	NP_001349403.1:p.Val177=
NM_001362475.1:c.255+242T=	NP_001349404.1:n.255+242T=
NM_001122630.2:c.497T= MANE Select	NP_001116102.1:p.Val166=
NM_001122631.2:c.497T=	NP_001116103.1:p.Val166=
NM_001362474.2:c.530T=	NP_001349403.1:p.Val177=
NM_001362475.2:c.255+242T=	NP_001349404.1:n.255+242T=