Canonical Allele Identifier: CA645552445

Gene: CDKN2A

Linked Data

• COSMIC: COSM85567

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971021_21971027del , CM000671.2:g.21971021_21971027del	GRCh38
NC_000009.11:g.21971020_21971026del , CM000671.1:g.21971020_21971026del	GRCh37
NC_000009.10:g.21961020_21961026del	NCBI36
NG_007485.1:g.28468_28474del , LRG_11:g.28468_28474del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.335_341del MANE Select	ENSP00000307101.5:p.Arg112ProfsTer?
ENST00000404796.3:c.348-58412_348-58406del	ENSP00000385916.2:n.348-58412_348-58406de...
ENST00000579755.2:c.378_384del MANE Plus Clinical	ENSP00000462950.1:p.Ser127ValfsTer?
ENST00000304494.9:c.335_341del	ENSP00000307101.5:p.Arg112ProfsTer?
ENST00000361570.4:c.377_383del	ENSP00000355153.4:p.Arg126ProfsTer?
ENST00000380150.2:n.309_315del
ENST00000380151.3:c.609_615del	ENSP00000369496.3:n.609_615del
ENST00000404796.2:c.348-58412_348-58406del	ENSP00000385916.2:n.348-58412_348-58406de...
ENST00000479692.2:c.182_188del	ENSP00000466887.1:p.Arg61ProfsTer?
ENST00000494262.5:c.182_188del	ENSP00000464952.1:p.Arg61ProfsTer?
ENST00000497750.1:c.182_188del	ENSP00000468510.1:p.Arg61ProfsTer?
ENST00000498124.1:c.335_341del	ENSP00000418915.1:p.Arg112ProfsTer?
ENST00000498628.6:c.182_188del	ENSP00000467857.1:p.Arg61ProfsTer?
ENST00000530628.2:c.378_384del	ENSP00000432664.2:p.Ser127ValfsTer25
ENST00000578845.2:c.182_188del	ENSP00000467390.1:p.Arg61ProfsTer?
ENST00000579122.1:c.335_341del	ENSP00000464202.1:p.Arg112ProfsTer19
ENST00000579755.1:c.378_384del	ENSP00000462950.1:p.Ser127ValfsTer?
NM_000077.4:c.335_341del , LRG_11t1:c.335_341del	NP_000068.1:p.Arg112ProfsTer?
NM_001195132.1:c.335_341del	NP_001182061.1:p.Arg112ProfsTer?
NM_058195.3:c.378_384del , LRG_11t2:c.378_384del	NP_478102.2:p.Ser127ValfsTer?
NM_058197.4:c.609_615del	NP_478104.2:n.609_615del
XM_005251343.1:c.182_188del	XP_005251400.1:p.Arg61ProfsTer?
XM_011517675.1:c.335_341del	XP_011515977.1:p.Arg112ProfsTer?
XM_011517676.1:c.335_341del	XP_011515978.1:p.Arg112ProfsTer?
XM_011517679.1:c.182_188del	XP_011515981.1:p.Arg61ProfsTer?
XR_929159.1:n.736_742del
XR_929161.1:n.525_531del
XR_929162.1:n.525_531del
XR_929163.1:n.474_480del
XR_929164.1:n.257_263del
NM_001363763.1:c.182_188del	NP_001350692.1:p.Arg61ProfsTer?
XM_011517675.2:c.335_341del	XP_011515977.1:p.Arg112ProfsTer?
XM_011517676.2:c.335_341del	XP_011515978.1:p.Arg112ProfsTer?
XR_929159.2:n.665_671del
NM_001363763.2:c.182_188del	NP_001350692.1:p.Arg61ProfsTer?
NM_000077.5:c.335_341del MANE Select	NP_000068.1:p.Arg112ProfsTer?
NM_001195132.2:c.335_341del	NP_001182061.1:p.Arg112ProfsTer?
NM_058195.4:c.378_384del MANE Plus Clinical	NP_478102.2:p.Ser127ValfsTer?
NM_058197.5:c.*258_*264del	NP_478104.2:n.*258_*264del