Canonical Allele Identifier: CA1839162259
Gene: CDKN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21971146_21971184delinsGTTGGGCTCCGCGCCGTGGAGCAGCAGCAGCTCCGCCAC , CM000671.2:g.21971146_21971184delinsGTTGGGCTCCGCGCCGTGGAGCAGCAGCAGCTCCGCCAC GRCh38
NC_000009.11:g.21971145_21971183delinsGTTGGGCTCCGCGCCGTGGAGCAGCAGCAGCTCCGCCAC , CM000671.1:g.21971145_21971183delinsGTTGGGCTCCGCGCCGTGGAGCAGCAGCAGCTCCGCCAC GRCh37
NC_000009.10:g.21961145_21961183delinsGTTGGGCTCCGCGCCGTGGAGCAGCAGCAGCTCCGCCAC NCBI36
NG_007485.1:g.28308_28346delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC , LRG_11:g.28308_28346delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000304494.10:c.175_213delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC MANE Select ENSP00000307101.5:p.Val59=
ENST00000404796.3:c.348-58287_348-58249delinsGTTGGGCTCCGCGCCGTGGAGCAGCAGCAGCTCCGCCAC ENSP00000385916.2:n.348-58287_348-58249de...
ENST00000579755.2:c.218_256delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC MANE Plus Clinical ENSP00000462950.1:p.Ser73=
ENST00000304494.9:c.175_213delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC ENSP00000307101.5:p.Val59=
ENST00000361570.4:c.218_256delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC ENSP00000355153.4:p.Ser73=
ENST00000380150.2:n.149_187delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC
ENST00000380151.3:c.449_487delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC ENSP00000369496.3:n.449_487delinsGTGGCGGA...
ENST00000404796.2:c.348-58287_348-58249delinsGTTGGGCTCCGCGCCGTGGAGCAGCAGCAGCTCCGCCAC ENSP00000385916.2:n.348-58287_348-58249de...
ENST00000479692.2:c.22_60delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC ENSP00000466887.1:p.Val8=
ENST00000494262.5:c.22_60delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC ENSP00000464952.1:p.Val8=
ENST00000497750.1:c.22_60delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC ENSP00000468510.1:p.Val8=
ENST00000498124.1:c.175_213delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC ENSP00000418915.1:p.Val59=
ENST00000498628.6:c.22_60delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC ENSP00000467857.1:p.Val8=
ENST00000530628.2:c.218_256delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC ENSP00000432664.2:p.Ser73=
ENST00000578845.2:c.22_60delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC ENSP00000467390.1:p.Val8=
ENST00000579122.1:c.175_213delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC ENSP00000464202.1:p.Val59=
ENST00000579755.1:c.218_256delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC ENSP00000462950.1:p.Ser73=
NM_000077.4:c.175_213delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC , LRG_11t1:c.175_213delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC NP_000068.1:p.Val59=
NM_001195132.1:c.175_213delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC NP_001182061.1:p.Val59=
NM_058195.3:c.218_256delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC , LRG_11t2:c.218_256delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC NP_478102.2:p.Ser73=
NM_058197.4:c.449_487delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC NP_478104.2:n.449_487delinsGTGGCGGAGCTGCT...
XM_005251343.1:c.22_60delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC XP_005251400.1:p.Val8=
XM_011517675.1:c.175_213delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC XP_011515977.1:p.Val59=
XM_011517676.1:c.175_213delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC XP_011515978.1:p.Val59=
XM_011517679.1:c.22_60delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC XP_011515981.1:p.Val8=
XR_929159.1:n.576_614delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC
XR_929161.1:n.365_403delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC
XR_929162.1:n.365_403delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC
XR_929163.1:n.314_352delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC
XR_929164.1:n.97_135delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC
NM_001363763.1:c.22_60delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC NP_001350692.1:p.Val8=
XM_011517675.2:c.175_213delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC XP_011515977.1:p.Val59=
XM_011517676.2:c.175_213delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC XP_011515978.1:p.Val59=
XR_929159.2:n.505_543delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC
NM_001363763.2:c.22_60delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC NP_001350692.1:p.Val8=
NM_000077.5:c.175_213delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC MANE Select NP_000068.1:p.Val59=
NM_001195132.2:c.175_213delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC NP_001182061.1:p.Val59=
NM_058195.4:c.218_256delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC MANE Plus Clinical NP_478102.2:p.Ser73=
NM_058197.5:c.*98_*136delinsGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAAC NP_478104.2:n.*98_*136delinsGTGGCGGAGCTGC...