Canonical Allele Identifier: CA379147654
Gene: CDKN1C HGNC NCBI

Linked Data

ClinVar Variation Id: 2031792
ClinVar RCV Id: RCV002867481
gnomAD v4: 11-2885357-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2885357C>A , CM000673.2:g.2885357C>A GRCh38
NC_000011.9:g.2906587C>A , CM000673.1:g.2906587C>A GRCh37
NC_000011.8:g.2863163C>A NCBI36
NG_008022.1:g.5409G>T , LRG_533:g.5409G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000681969.1:n.142+277G>T
ENST00000380725.2:c.100G>T ENSP00000370101.1:p.Glu34Ter
ENST00000414822.8:c.133G>T ENSP00000413720.3:p.Glu45Ter
ENST00000430149.3:c.133G>T ENSP00000411552.2:p.Glu45Ter
ENST00000440480.8:c.100G>T MANE Select ENSP00000411257.2:p.Glu34Ter
ENST00000647251.1:c.100G>T ENSP00000496631.1:p.Glu34Ter
ENST00000380725.1:c.100G>T ENSP00000370101.1:p.Glu34Ter
ENST00000414822.7:c.133G>T ENSP00000413720.3:p.Glu45Ter
ENST00000430149.2:c.133G>T ENSP00000411552.2:p.Glu45Ter
ENST00000440480.6:c.100G>T ENSP00000411257.2:p.Glu34Ter
NM_000076.2:c.133G>T , LRG_533t1:c.133G>T NP_000067.1:p.Glu45Ter
NM_001122630.1:c.100G>T NP_001116102.1:p.Glu34Ter
NM_001122631.1:c.100G>T NP_001116103.1:p.Glu34Ter
XM_005252732.3:c.100G>T XP_005252789.1:p.Glu34Ter
NM_001362474.1:c.133G>T NP_001349403.1:p.Glu45Ter
NM_001362475.1:c.100G>T NP_001349404.1:p.Glu34Ter
NM_001122630.2:c.100G>T MANE Select NP_001116102.1:p.Glu34Ter
NM_001122631.2:c.100G>T NP_001116103.1:p.Glu34Ter
NM_001362474.2:c.133G>T NP_001349403.1:p.Glu45Ter
NM_001362475.2:c.100G>T NP_001349404.1:p.Glu34Ter