Canonical Allele Identifier: CA2695210497

Gene: CDKN2A

Linked Data

• ClinVar Variation Id: 3230258
• ClinVar RCV Id: RCV004520409

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974785_21974787delinsGTGGCCGTGGCCAGCCACGG , CM000671.2:g.21974785_21974787delinsGTGGCCGTGGCCAGCCACGG	GRCh38
NC_000009.11:g.21974784_21974786delinsGTGGCCGTGGCCAGCCACGG , CM000671.1:g.21974784_21974786delinsGTGGCCGTGGCCAGCCACGG	GRCh37
NC_000009.10:g.21964784_21964786delinsGTGGCCGTGGCCAGCCACGG	NCBI36
NG_007485.1:g.24705_24707delinsCCGTGGCTGGCCACGGCCAC , LRG_11:g.24705_24707delinsCCGTGGCTGGCCACGGCCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.41_43delinsCCGTGGCTGGCCACGGCCAC MANE Select	ENSP00000307101.5:p.Asp14AlafsTer18
ENST00000404796.3:c.348-54648_348-54646delinsGTGGCCGTGGCCAGCCACGG	ENSP00000385916.2:n.348-54648_348-54646delinsGTGGCCGTGGCCAGCC...
ENST00000579755.2:c.194-3579_194-3577delinsCCGTGGCTGGCCACGGCCAC MANE Plus Clinical	ENSP00000462950.1:n.194-3579_194-3577delinsCCGTGGCTGGCCACGGCC...
ENST00000304494.9:c.41_43delinsCCGTGGCTGGCCACGGCCAC	ENSP00000307101.5:p.Asp14AlafsTer18
ENST00000361570.4:c.194-3579_194-3577delinsCCGTGGCTGGCCACGGCCAC	ENSP00000355153.4:n.194-3579_194-3577delinsCCGTGGCTGGCCACGGCC...
ENST00000380151.3:c.41_43delinsCCGTGGCTGGCCACGGCCAC	ENSP00000369496.3:p.Asp14AlafsTer18
ENST00000404796.2:c.348-54648_348-54646delinsGTGGCCGTGGCCAGCCACGG	ENSP00000385916.2:n.348-54648_348-54646delinsGTGGCCGTGGCCAGCC...
ENST00000494262.5:c.-3-3579_-3-3577delinsCCGTGGCTGGCCACGGCCAC	ENSP00000464952.1:n.-3-3579_-3-3577delinsCCGTGGCTGGCCACGGCCAC...
ENST00000498124.1:c.41_43delinsCCGTGGCTGGCCACGGCCAC	ENSP00000418915.1:p.Asp14AlafsTer18
ENST00000498628.6:c.-3-3579_-3-3577delinsCCGTGGCTGGCCACGGCCAC	ENSP00000467857.1:n.-3-3579_-3-3577delinsCCGTGGCTGGCCACGGCCAC...
ENST00000530628.2:c.194-3579_194-3577delinsCCGTGGCTGGCCACGGCCAC	ENSP00000432664.2:n.194-3579_194-3577delinsCCGTGGCTGGCCACGGCC...
ENST00000579122.1:c.41_43delinsCCGTGGCTGGCCACGGCCAC	ENSP00000464202.1:p.Asp14AlafsTer18
ENST00000579755.1:c.194-3579_194-3577delinsCCGTGGCTGGCCACGGCCAC	ENSP00000462950.1:n.194-3579_194-3577delinsCCGTGGCTGGCCACGGCC...
NM_000077.4:c.41_43delinsCCGTGGCTGGCCACGGCCAC , LRG_11t1:c.41_43delinsCCGTGGCTGGCCACGGCCAC	NP_000068.1:p.Asp14AlafsTer18
NM_001195132.1:c.41_43delinsCCGTGGCTGGCCACGGCCAC	NP_001182061.1:p.Asp14AlafsTer18
NM_058195.3:c.194-3579_194-3577delinsCCGTGGCTGGCCACGGCCAC , LRG_11t2:c.194-3579_194-3577delinsCCGTGGCTGGCCACGGCCAC	NP_478102.2:n.194-3579_194-3577delinsCCGTGGCTGGCCACGGCCAC
NM_058197.4:c.41_43delinsCCGTGGCTGGCCACGGCCAC	NP_478104.2:p.Asp14AlafsTer18
XM_011517675.1:c.41_43delinsCCGTGGCTGGCCACGGCCAC	XP_011515977.1:p.Asp14AlafsTer18
XM_011517676.1:c.41_43delinsCCGTGGCTGGCCACGGCCAC	XP_011515978.1:p.Asp14AlafsTer18
XM_011517679.1:c.-3-3579_-3-3577delinsCCGTGGCTGGCCACGGCCAC	XP_011515981.1:n.-3-3579_-3-3577delinsCCGTGGCTGGCCACGGCCAC
XR_929159.1:n.442_444delinsCCGTGGCTGGCCACGGCCAC
XR_929161.1:n.341-3579_341-3577delinsCCGTGGCTGGCCACGGCCAC
XR_929162.1:n.341-3579_341-3577delinsCCGTGGCTGGCCACGGCCAC
XR_929163.1:n.290-3579_290-3577delinsCCGTGGCTGGCCACGGCCAC
NM_001363763.1:c.-3-3579_-3-3577delinsCCGTGGCTGGCCACGGCCAC	NP_001350692.1:n.-3-3579_-3-3577delinsCCGTGGCTGGCCACGGCCAC
XM_011517675.2:c.41_43delinsCCGTGGCTGGCCACGGCCAC	XP_011515977.1:p.Asp14AlafsTer18
XM_011517676.2:c.41_43delinsCCGTGGCTGGCCACGGCCAC	XP_011515978.1:p.Asp14AlafsTer18
XR_929159.2:n.371_373delinsCCGTGGCTGGCCACGGCCAC
NM_001363763.2:c.-3-3579_-3-3577delinsCCGTGGCTGGCCACGGCCAC	NP_001350692.1:n.-3-3579_-3-3577delinsCCGTGGCTGGCCACGGCCAC
NM_000077.5:c.41_43delinsCCGTGGCTGGCCACGGCCAC MANE Select	NP_000068.1:p.Asp14AlafsTer18
NM_001195132.2:c.41_43delinsCCGTGGCTGGCCACGGCCAC	NP_001182061.1:p.Asp14AlafsTer18
NM_058195.4:c.194-3579_194-3577delinsCCGTGGCTGGCCACGGCCAC MANE Plus Clinical	NP_478102.2:n.194-3579_194-3577delinsCCGTGGCTGGCCACGGCCAC
NM_058197.5:c.41_43delinsCCGTGGCTGGCCACGGCCAC	NP_478104.2:p.Asp14AlafsTer18