Canonical Allele Identifier: CA645552612
Gene: CDKN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1171238
ClinVar RCV Id: RCV001524193
dbSNP Id: rs398123152

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21974726del , CM000671.2:g.21974726del GRCh38
NC_000009.11:g.21974725del , CM000671.1:g.21974725del GRCh37
NC_000009.10:g.21964725del NCBI36
NG_007485.1:g.24770del , LRG_11:g.24770del

Transcript Alleles

HGVS Amino-acid Change
ENST00000304494.10:c.106del MANE Select ENSP00000307101.5:p.Ala36ArgfsTer17
ENST00000404796.3:c.348-54707del ENSP00000385916.2:n.348-54707del
ENST00000579755.2:c.194-3514del MANE Plus Clinical ENSP00000462950.1:n.194-3514del
ENST00000304494.9:c.106del ENSP00000307101.5:p.Ala36ArgfsTer17
ENST00000361570.4:c.194-3514del ENSP00000355153.4:n.194-3514del
ENST00000380151.3:c.106del ENSP00000369496.3:p.Ala36ArgfsTer?
ENST00000404796.2:c.348-54707del ENSP00000385916.2:n.348-54707del
ENST00000494262.5:c.-3-3514del ENSP00000464952.1:n.-3-3514del
ENST00000498124.1:c.106del ENSP00000418915.1:p.Ala36ArgfsTer17
ENST00000498628.6:c.-3-3514del ENSP00000467857.1:n.-3-3514del
ENST00000530628.2:c.194-3514del ENSP00000432664.2:n.194-3514del
ENST00000579122.1:c.106del ENSP00000464202.1:p.Ala36ArgfsTer17
ENST00000579755.1:c.194-3514del ENSP00000462950.1:n.194-3514del
NM_000077.4:c.106del , LRG_11t1:c.106del NP_000068.1:p.Ala36ArgfsTer17
NM_001195132.1:c.106del NP_001182061.1:p.Ala36ArgfsTer17
NM_058195.3:c.194-3514del , LRG_11t2:c.194-3514del NP_478102.2:n.194-3514del
NM_058197.4:c.106del NP_478104.2:p.Ala36ArgfsTer?
XM_011517675.1:c.106del XP_011515977.1:p.Ala36ArgfsTer17
XM_011517676.1:c.106del XP_011515978.1:p.Ala36ArgfsTer17
XM_011517679.1:c.-3-3514del XP_011515981.1:n.-3-3514del
XR_929159.1:n.507del
XR_929161.1:n.341-3514del
XR_929162.1:n.341-3514del
XR_929163.1:n.290-3514del
NM_001363763.1:c.-3-3514del NP_001350692.1:n.-3-3514del
XM_011517675.2:c.106del XP_011515977.1:p.Ala36ArgfsTer17
XM_011517676.2:c.106del XP_011515978.1:p.Ala36ArgfsTer17
XR_929159.2:n.436del
NM_001363763.2:c.-3-3514del NP_001350692.1:n.-3-3514del
NM_000077.5:c.106del MANE Select NP_000068.1:p.Ala36ArgfsTer17
NM_001195132.2:c.106del NP_001182061.1:p.Ala36ArgfsTer17
NM_058195.4:c.194-3514del MANE Plus Clinical NP_478102.2:n.194-3514del
NM_058197.5:c.106del NP_478104.2:p.Ala36ArgfsTer?