Canonical Allele Identifier: CA645552579

Gene: CDKN2A

Linked Data

• COSMIC: COSM303835 ; COSM303836 ; COSM303837

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971204_21971205insGC , CM000671.2:g.21971204_21971205insGC	GRCh38
NC_000009.11:g.21971203_21971204insGC , CM000671.1:g.21971203_21971204insGC	GRCh37
NC_000009.10:g.21961203_21961204insGC	NCBI36
NG_007485.1:g.28287_28288insGC , LRG_11:g.28287_28288insGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.154_155insGC MANE Select	ENSP00000307101.5:p.Met52SerfsTer2
ENST00000404796.3:c.348-58229_348-58228insGC	ENSP00000385916.2:n.348-58229_348-58228in...
ENST00000579755.2:c.197_198insGC MANE Plus Clinical	ENSP00000462950.1:p.His66GlnfsTer?
ENST00000304494.9:c.154_155insGC	ENSP00000307101.5:p.Met52SerfsTer2
ENST00000361570.4:c.197_198insGC	ENSP00000355153.4:p.His66GlnfsTer?
ENST00000380150.2:n.128_129insGC
ENST00000380151.3:c.428_429insGC	ENSP00000369496.3:n.428_429insGC
ENST00000404796.2:c.348-58229_348-58228insGC	ENSP00000385916.2:n.348-58229_348-58228in...
ENST00000479692.2:c.1_2insGC	ENSP00000466887.1:p.Met1SerfsTer2
ENST00000494262.5:c.1_2insGC	ENSP00000464952.1:p.Met1SerfsTer2
ENST00000497750.1:c.1_2insGC	ENSP00000468510.1:p.Met1SerfsTer2
ENST00000498124.1:c.154_155insGC	ENSP00000418915.1:p.Met52SerfsTer2
ENST00000498628.6:c.1_2insGC	ENSP00000467857.1:p.Met1SerfsTer2
ENST00000530628.2:c.197_198insGC	ENSP00000432664.2:p.His66GlnfsTer?
ENST00000578845.2:c.1_2insGC	ENSP00000467390.1:p.Met1SerfsTer2
ENST00000579122.1:c.154_155insGC	ENSP00000464202.1:p.Met52SerfsTer2
ENST00000579755.1:c.197_198insGC	ENSP00000462950.1:p.His66GlnfsTer?
NM_000077.4:c.154_155insGC , LRG_11t1:c.154_155insGC	NP_000068.1:p.Met52SerfsTer2
NM_001195132.1:c.154_155insGC	NP_001182061.1:p.Met52SerfsTer2
NM_058195.3:c.197_198insGC , LRG_11t2:c.197_198insGC	NP_478102.2:p.His66GlnfsTer?
NM_058197.4:c.428_429insGC	NP_478104.2:n.428_429insGC
XM_005251343.1:c.1_2insGC	XP_005251400.1:p.Met1SerfsTer2
XM_011517675.1:c.154_155insGC	XP_011515977.1:p.Met52SerfsTer2
XM_011517676.1:c.154_155insGC	XP_011515978.1:p.Met52SerfsTer2
XM_011517679.1:c.1_2insGC	XP_011515981.1:p.Met1SerfsTer2
XR_929159.1:n.555_556insGC
XR_929161.1:n.344_345insGC
XR_929162.1:n.344_345insGC
XR_929163.1:n.293_294insGC
XR_929164.1:n.76_77insGC
NM_001363763.1:c.1_2insGC	NP_001350692.1:p.Met1SerfsTer2
XM_011517675.2:c.154_155insGC	XP_011515977.1:p.Met52SerfsTer2
XM_011517676.2:c.154_155insGC	XP_011515978.1:p.Met52SerfsTer2
XR_929159.2:n.484_485insGC
NM_001363763.2:c.1_2insGC	NP_001350692.1:p.Met1SerfsTer2
NM_000077.5:c.154_155insGC MANE Select	NP_000068.1:p.Met52SerfsTer2
NM_001195132.2:c.154_155insGC	NP_001182061.1:p.Met52SerfsTer2
NM_058195.4:c.197_198insGC MANE Plus Clinical	NP_478102.2:p.His66GlnfsTer?
NM_058197.5:c.*77_*78insGC	NP_478104.2:n.*77_*78insGC