Canonical Allele Identifier: CA645552455

Gene: CDKN2A

Linked Data

• COSMIC: COSM33791

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971053_21971059del , CM000671.2:g.21971053_21971059del	GRCh38
NC_000009.11:g.21971052_21971058del , CM000671.1:g.21971052_21971058del	GRCh37
NC_000009.10:g.21961052_21961058del	NCBI36
NG_007485.1:g.28436_28442del , LRG_11:g.28436_28442del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.303_309del MANE Select	ENSP00000307101.5:p.Ala102TrpfsTer?
ENST00000404796.3:c.348-58380_348-58374del	ENSP00000385916.2:n.348-58380_348-58374del
ENST00000579755.2:c.346_352del MANE Plus Clinical	ENSP00000462950.1:p.Gly116LeufsTer?
ENST00000304494.9:c.303_309del	ENSP00000307101.5:p.Ala102TrpfsTer?
ENST00000361570.4:c.345_351del	ENSP00000355153.4:p.Ala116TrpfsTer?
ENST00000380150.2:n.277_283del
ENST00000380151.3:c.577_583del	ENSP00000369496.3:n.577_583del
ENST00000404796.2:c.348-58380_348-58374del	ENSP00000385916.2:n.348-58380_348-58374del
ENST00000479692.2:c.150_156del	ENSP00000466887.1:p.Ala51TrpfsTer?
ENST00000494262.5:c.150_156del	ENSP00000464952.1:p.Ala51TrpfsTer?
ENST00000497750.1:c.150_156del	ENSP00000468510.1:p.Ala51TrpfsTer?
ENST00000498124.1:c.303_309del	ENSP00000418915.1:p.Ala102TrpfsTer?
ENST00000498628.6:c.150_156del	ENSP00000467857.1:p.Ala51TrpfsTer?
ENST00000530628.2:c.346_352del	ENSP00000432664.2:p.Gly116LeufsTer?
ENST00000578845.2:c.150_156del	ENSP00000467390.1:p.Ala51TrpfsTer?
ENST00000579122.1:c.303_309del	ENSP00000464202.1:p.Ala102TrpfsTer29
ENST00000579755.1:c.346_352del	ENSP00000462950.1:p.Gly116LeufsTer?
NM_000077.4:c.303_309del , LRG_11t1:c.303_309del	NP_000068.1:p.Ala102TrpfsTer?
NM_001195132.1:c.303_309del	NP_001182061.1:p.Ala102TrpfsTer?
NM_058195.3:c.346_352del , LRG_11t2:c.346_352del	NP_478102.2:p.Gly116LeufsTer?
NM_058197.4:c.577_583del	NP_478104.2:n.577_583del
XM_005251343.1:c.150_156del	XP_005251400.1:p.Ala51TrpfsTer?
XM_011517675.1:c.303_309del	XP_011515977.1:p.Ala102TrpfsTer?
XM_011517676.1:c.303_309del	XP_011515978.1:p.Ala102TrpfsTer?
XM_011517679.1:c.150_156del	XP_011515981.1:p.Ala51TrpfsTer?
XR_929159.1:n.704_710del
XR_929161.1:n.493_499del
XR_929162.1:n.493_499del
XR_929163.1:n.442_448del
XR_929164.1:n.225_231del
NM_001363763.1:c.150_156del	NP_001350692.1:p.Ala51TrpfsTer?
XM_011517675.2:c.303_309del	XP_011515977.1:p.Ala102TrpfsTer?
XM_011517676.2:c.303_309del	XP_011515978.1:p.Ala102TrpfsTer?
XR_929159.2:n.633_639del
NM_001363763.2:c.150_156del	NP_001350692.1:p.Ala51TrpfsTer?
NM_000077.5:c.303_309del MANE Select	NP_000068.1:p.Ala102TrpfsTer?
NM_001195132.2:c.303_309del	NP_001182061.1:p.Ala102TrpfsTer?
NM_058195.4:c.346_352del MANE Plus Clinical	NP_478102.2:p.Gly116LeufsTer?
NM_058197.5:c.*226_*232del	NP_478104.2:n.*226_*232del