Canonical Allele Identifier: CA645552454

Gene: CDKN2A

Linked Data

• COSMIC: COSM13676

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971050_21971088del , CM000671.2:g.21971050_21971088del	GRCh38
NC_000009.11:g.21971049_21971087del , CM000671.1:g.21971049_21971087del	GRCh37
NC_000009.10:g.21961049_21961087del	NCBI36
NG_007485.1:g.28410_28448del , LRG_11:g.28410_28448del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.277_315del MANE Select	ENSP00000307101.5:p.Thr93_Asp105del
ENST00000404796.3:c.348-58383_348-58345del	ENSP00000385916.2:n.348-58383_348-58345de...
ENST00000579755.2:c.320_358del MANE Plus Clinical	ENSP00000462950.1:p.His107_Gly119del
ENST00000304494.9:c.277_315del	ENSP00000307101.5:p.Thr93_Asp105del
ENST00000361570.4:c.319_357del	ENSP00000355153.4:p.Thr107_Asp119del
ENST00000380150.2:n.251_289del
ENST00000380151.3:c.551_589del	ENSP00000369496.3:n.551_589del
ENST00000404796.2:c.348-58383_348-58345del	ENSP00000385916.2:n.348-58383_348-58345de...
ENST00000479692.2:c.124_162del	ENSP00000466887.1:p.Thr42_Asp54del
ENST00000494262.5:c.124_162del	ENSP00000464952.1:p.Thr42_Asp54del
ENST00000497750.1:c.124_162del	ENSP00000468510.1:p.Thr42_Asp54del
ENST00000498124.1:c.277_315del	ENSP00000418915.1:p.Thr93_Asp105del
ENST00000498628.6:c.124_162del	ENSP00000467857.1:p.Thr42_Asp54del
ENST00000530628.2:c.320_358del	ENSP00000432664.2:p.His107_Gly119del
ENST00000578845.2:c.124_162del	ENSP00000467390.1:p.Thr42_Asp54del
ENST00000579122.1:c.277_315del	ENSP00000464202.1:p.Thr93_Asp105del
ENST00000579755.1:c.320_358del	ENSP00000462950.1:p.His107_Gly119del
NM_000077.4:c.277_315del , LRG_11t1:c.277_315del	NP_000068.1:p.Thr93_Asp105del
NM_001195132.1:c.277_315del	NP_001182061.1:p.Thr93_Asp105del
NM_058195.3:c.320_358del , LRG_11t2:c.320_358del	NP_478102.2:p.His107_Gly119del
NM_058197.4:c.551_589del	NP_478104.2:n.551_589del
XM_005251343.1:c.124_162del	XP_005251400.1:p.Thr42_Asp54del
XM_011517675.1:c.277_315del	XP_011515977.1:p.Thr93_Asp105del
XM_011517676.1:c.277_315del	XP_011515978.1:p.Thr93_Asp105del
XM_011517679.1:c.124_162del	XP_011515981.1:p.Thr42_Asp54del
XR_929159.1:n.678_716del
XR_929161.1:n.467_505del
XR_929162.1:n.467_505del
XR_929163.1:n.416_454del
XR_929164.1:n.199_237del
NM_001363763.1:c.124_162del	NP_001350692.1:p.Thr42_Asp54del
XM_011517675.2:c.277_315del	XP_011515977.1:p.Thr93_Asp105del
XM_011517676.2:c.277_315del	XP_011515978.1:p.Thr93_Asp105del
XR_929159.2:n.607_645del
NM_001363763.2:c.124_162del	NP_001350692.1:p.Thr42_Asp54del
NM_000077.5:c.277_315del MANE Select	NP_000068.1:p.Thr93_Asp105del
NM_001195132.2:c.277_315del	NP_001182061.1:p.Thr93_Asp105del
NM_058195.4:c.320_358del MANE Plus Clinical	NP_478102.2:p.His107_Gly119del
NM_058197.5:c.*200_*238del	NP_478104.2:n.*200_*238del