Canonical Allele Identifier: CA645552463

Gene: CDKN2A

Linked Data

• COSMIC: COSM3736957

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971065_21971073del , CM000671.2:g.21971065_21971073del	GRCh38
NC_000009.11:g.21971064_21971072del , CM000671.1:g.21971064_21971072del	GRCh37
NC_000009.10:g.21961064_21961072del	NCBI36
NG_007485.1:g.28419_28427del , LRG_11:g.28419_28427del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.286_294del MANE Select	ENSP00000307101.5:p.Val96_His98del
ENST00000404796.3:c.348-58368_348-58360del	ENSP00000385916.2:n.348-58368_348-58360del
ENST00000579755.2:c.329_337del MANE Plus Clinical	ENSP00000462950.1:p.Gly110_Pro113delinsAla
ENST00000304494.9:c.286_294del	ENSP00000307101.5:p.Val96_His98del
ENST00000361570.4:c.328_336del	ENSP00000355153.4:p.Val110_His112del
ENST00000380150.2:n.260_268del
ENST00000380151.3:c.560_568del	ENSP00000369496.3:n.560_568del
ENST00000404796.2:c.348-58368_348-58360del	ENSP00000385916.2:n.348-58368_348-58360del
ENST00000479692.2:c.133_141del	ENSP00000466887.1:p.Val45_His47del
ENST00000494262.5:c.133_141del	ENSP00000464952.1:p.Val45_His47del
ENST00000497750.1:c.133_141del	ENSP00000468510.1:p.Val45_His47del
ENST00000498124.1:c.286_294del	ENSP00000418915.1:p.Val96_His98del
ENST00000498628.6:c.133_141del	ENSP00000467857.1:p.Val45_His47del
ENST00000530628.2:c.329_337del	ENSP00000432664.2:p.Gly110_Pro113delinsAla
ENST00000578845.2:c.133_141del	ENSP00000467390.1:p.Val45_His47del
ENST00000579122.1:c.286_294del	ENSP00000464202.1:p.Val96_His98del
ENST00000579755.1:c.329_337del	ENSP00000462950.1:p.Gly110_Pro113delinsAla
NM_000077.4:c.286_294del , LRG_11t1:c.286_294del	NP_000068.1:p.Val96_His98del
NM_001195132.1:c.286_294del	NP_001182061.1:p.Val96_His98del
NM_058195.3:c.329_337del , LRG_11t2:c.329_337del	NP_478102.2:p.Gly110_Pro113delinsAla
NM_058197.4:c.560_568del	NP_478104.2:n.560_568del
XM_005251343.1:c.133_141del	XP_005251400.1:p.Val45_His47del
XM_011517675.1:c.286_294del	XP_011515977.1:p.Val96_His98del
XM_011517676.1:c.286_294del	XP_011515978.1:p.Val96_His98del
XM_011517679.1:c.133_141del	XP_011515981.1:p.Val45_His47del
XR_929159.1:n.687_695del
XR_929161.1:n.476_484del
XR_929162.1:n.476_484del
XR_929163.1:n.425_433del
XR_929164.1:n.208_216del
NM_001363763.1:c.133_141del	NP_001350692.1:p.Val45_His47del
XM_011517675.2:c.286_294del	XP_011515977.1:p.Val96_His98del
XM_011517676.2:c.286_294del	XP_011515978.1:p.Val96_His98del
XR_929159.2:n.616_624del
NM_001363763.2:c.133_141del	NP_001350692.1:p.Val45_His47del
NM_000077.5:c.286_294del MANE Select	NP_000068.1:p.Val96_His98del
NM_001195132.2:c.286_294del	NP_001182061.1:p.Val96_His98del
NM_058195.4:c.329_337del MANE Plus Clinical	NP_478102.2:p.Gly110_Pro113delinsAla
NM_058197.5:c.*209_*217del	NP_478104.2:n.*209_*217del