Canonical Allele Identifier: CA1839161058
Gene: CDKN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21971003_21971019delinsTCAGCCAGGTCCACGGG , CM000671.2:g.21971003_21971019delinsTCAGCCAGGTCCACGGG GRCh38
NC_000009.11:g.21971002_21971018delinsTCAGCCAGGTCCACGGG , CM000671.1:g.21971002_21971018delinsTCAGCCAGGTCCACGGG GRCh37
NC_000009.10:g.21961002_21961018delinsTCAGCCAGGTCCACGGG NCBI36
NG_007485.1:g.28473_28489delinsCCCGTGGACCTGGCTGA , LRG_11:g.28473_28489delinsCCCGTGGACCTGGCTGA

Transcript Alleles

HGVS Amino-acid change
ENST00000304494.10:c.340_356delinsCCCGTGGACCTGGCTGA MANE Select ENSP00000307101.5:p.Pro114=
ENST00000404796.3:c.348-58430_348-58414delinsTCAGCCAGGTCCACGGG ENSP00000385916.2:n.348-58430_348-58414de...
ENST00000579755.2:c.383_399delinsCCCGTGGACCTGGCTGA MANE Plus Clinical ENSP00000462950.1:p.Ala128=
ENST00000304494.9:c.340_356delinsCCCGTGGACCTGGCTGA ENSP00000307101.5:p.Pro114=
ENST00000361570.4:c.382_398delinsCCCGTGGACCTGGCTGA ENSP00000355153.4:p.Pro128=
ENST00000380150.2:n.314_330delinsCCCGTGGACCTGGCTGA
ENST00000380151.3:c.614_630delinsCCCGTGGACCTGGCTGA ENSP00000369496.3:n.614_630delinsCCCGTGGA...
ENST00000404796.2:c.348-58430_348-58414delinsTCAGCCAGGTCCACGGG ENSP00000385916.2:n.348-58430_348-58414de...
ENST00000479692.2:c.187_203delinsCCCGTGGACCTGGCTGA ENSP00000466887.1:p.Pro63=
ENST00000494262.5:c.187_203delinsCCCGTGGACCTGGCTGA ENSP00000464952.1:p.Pro63=
ENST00000497750.1:c.187_203delinsCCCGTGGACCTGGCTGA ENSP00000468510.1:p.Pro63=
ENST00000498124.1:c.340_356delinsCCCGTGGACCTGGCTGA ENSP00000418915.1:p.Pro114=
ENST00000498628.6:c.187_203delinsCCCGTGGACCTGGCTGA ENSP00000467857.1:p.Pro63=
ENST00000530628.2:c.383_399delinsCCCGTGGACCTGGCTGA ENSP00000432664.2:p.Ala128=
ENST00000578845.2:c.187_203delinsCCCGTGGACCTGGCTGA ENSP00000467390.1:p.Pro63=
ENST00000579122.1:c.340_356delinsCCCGTGGACCTGGCTGA ENSP00000464202.1:p.Pro114=
ENST00000579755.1:c.383_399delinsCCCGTGGACCTGGCTGA ENSP00000462950.1:p.Ala128=
NM_000077.4:c.340_356delinsCCCGTGGACCTGGCTGA , LRG_11t1:c.340_356delinsCCCGTGGACCTGGCTGA NP_000068.1:p.Pro114=
NM_001195132.1:c.340_356delinsCCCGTGGACCTGGCTGA NP_001182061.1:p.Pro114=
NM_058195.3:c.383_399delinsCCCGTGGACCTGGCTGA , LRG_11t2:c.383_399delinsCCCGTGGACCTGGCTGA NP_478102.2:p.Ala128=
NM_058197.4:c.614_630delinsCCCGTGGACCTGGCTGA NP_478104.2:n.614_630delinsCCCGTGGACCTGGC...
XM_005251343.1:c.187_203delinsCCCGTGGACCTGGCTGA XP_005251400.1:p.Pro63=
XM_011517675.1:c.340_356delinsCCCGTGGACCTGGCTGA XP_011515977.1:p.Pro114=
XM_011517676.1:c.340_356delinsCCCGTGGACCTGGCTGA XP_011515978.1:p.Pro114=
XM_011517679.1:c.187_203delinsCCCGTGGACCTGGCTGA XP_011515981.1:p.Pro63=
XR_929159.1:n.741_757delinsCCCGTGGACCTGGCTGA
XR_929161.1:n.530_546delinsCCCGTGGACCTGGCTGA
XR_929162.1:n.530_546delinsCCCGTGGACCTGGCTGA
XR_929163.1:n.479_495delinsCCCGTGGACCTGGCTGA
XR_929164.1:n.262_278delinsCCCGTGGACCTGGCTGA
NM_001363763.1:c.187_203delinsCCCGTGGACCTGGCTGA NP_001350692.1:p.Pro63=
XM_011517675.2:c.340_356delinsCCCGTGGACCTGGCTGA XP_011515977.1:p.Pro114=
XM_011517676.2:c.340_356delinsCCCGTGGACCTGGCTGA XP_011515978.1:p.Pro114=
XR_929159.2:n.670_686delinsCCCGTGGACCTGGCTGA
NM_001363763.2:c.187_203delinsCCCGTGGACCTGGCTGA NP_001350692.1:p.Pro63=
NM_000077.5:c.340_356delinsCCCGTGGACCTGGCTGA MANE Select NP_000068.1:p.Pro114=
NM_001195132.2:c.340_356delinsCCCGTGGACCTGGCTGA NP_001182061.1:p.Pro114=
NM_058195.4:c.383_399delinsCCCGTGGACCTGGCTGA MANE Plus Clinical NP_478102.2:p.Ala128=
NM_058197.5:c.*263_*279delinsCCCGTGGACCTGGCTGA NP_478104.2:n.*263_*279delinsCCCGTGGACCTG...