Canonical Allele Identifier: CA645552614

Gene: CDKN2A

Linked Data

• COSMIC: COSM13822

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974727_21974744del , CM000671.2:g.21974727_21974744del	GRCh38
NC_000009.11:g.21974726_21974743del , CM000671.1:g.21974726_21974743del	GRCh37
NC_000009.10:g.21964726_21964743del	NCBI36
NG_007485.1:g.24749_24766del , LRG_11:g.24749_24766del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.85_102del MANE Select	ENSP00000307101.5:p.Arg29_Ala34del
ENST00000404796.3:c.348-54706_348-54689del	ENSP00000385916.2:n.348-54706_348-54689del
ENST00000579755.2:c.194-3535_194-3518del MANE Plus Clinical	ENSP00000462950.1:n.194-3535_194-3518del
ENST00000304494.9:c.85_102del	ENSP00000307101.5:p.Arg29_Ala34del
ENST00000361570.4:c.194-3535_194-3518del	ENSP00000355153.4:n.194-3535_194-3518del
ENST00000380151.3:c.85_102del	ENSP00000369496.3:p.Arg29_Ala34del
ENST00000404796.2:c.348-54706_348-54689del	ENSP00000385916.2:n.348-54706_348-54689del
ENST00000494262.5:c.-3-3535_-3-3518del	ENSP00000464952.1:n.-3-3535_-3-3518del
ENST00000498124.1:c.85_102del	ENSP00000418915.1:p.Arg29_Ala34del
ENST00000498628.6:c.-3-3535_-3-3518del	ENSP00000467857.1:n.-3-3535_-3-3518del
ENST00000530628.2:c.194-3535_194-3518del	ENSP00000432664.2:n.194-3535_194-3518del
ENST00000579122.1:c.85_102del	ENSP00000464202.1:p.Arg29_Ala34del
ENST00000579755.1:c.194-3535_194-3518del	ENSP00000462950.1:n.194-3535_194-3518del
NM_000077.4:c.85_102del , LRG_11t1:c.85_102del	NP_000068.1:p.Arg29_Ala34del
NM_001195132.1:c.85_102del	NP_001182061.1:p.Arg29_Ala34del
NM_058195.3:c.194-3535_194-3518del , LRG_11t2:c.194-3535_194-3518del	NP_478102.2:n.194-3535_194-3518del
NM_058197.4:c.85_102del	NP_478104.2:p.Arg29_Ala34del
XM_011517675.1:c.85_102del	XP_011515977.1:p.Arg29_Ala34del
XM_011517676.1:c.85_102del	XP_011515978.1:p.Arg29_Ala34del
XM_011517679.1:c.-3-3535_-3-3518del	XP_011515981.1:n.-3-3535_-3-3518del
XR_929159.1:n.486_503del
XR_929161.1:n.341-3535_341-3518del
XR_929162.1:n.341-3535_341-3518del
XR_929163.1:n.290-3535_290-3518del
NM_001363763.1:c.-3-3535_-3-3518del	NP_001350692.1:n.-3-3535_-3-3518del
XM_011517675.2:c.85_102del	XP_011515977.1:p.Arg29_Ala34del
XM_011517676.2:c.85_102del	XP_011515978.1:p.Arg29_Ala34del
XR_929159.2:n.415_432del
NM_001363763.2:c.-3-3535_-3-3518del	NP_001350692.1:n.-3-3535_-3-3518del
NM_000077.5:c.85_102del MANE Select	NP_000068.1:p.Arg29_Ala34del
NM_001195132.2:c.85_102del	NP_001182061.1:p.Arg29_Ala34del
NM_058195.4:c.194-3535_194-3518del MANE Plus Clinical	NP_478102.2:n.194-3535_194-3518del
NM_058197.5:c.85_102del	NP_478104.2:p.Arg29_Ala34del