Canonical Allele Identifier: CA645552475

Gene: CDKN2A

Linked Data

• COSMIC: COSM4993345 ; COSM4993346 ; COSM4993347 ; COSM4993348

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971100_21971102del , CM000671.2:g.21971100_21971102del	GRCh38
NC_000009.11:g.21971099_21971101del , CM000671.1:g.21971099_21971101del	GRCh37
NC_000009.10:g.21961099_21961101del	NCBI36
NG_007485.1:g.28390_28392del , LRG_11:g.28390_28392del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.257_259del MANE Select	ENSP00000307101.5:p.Ala86_Arg87delinsGly
ENST00000404796.3:c.348-58333_348-58331del	ENSP00000385916.2:n.348-58333_348-58331de...
ENST00000579755.2:c.300_302del MANE Plus Clinical	ENSP00000462950.1:p.Cys100_Pro101delinsTr...
ENST00000304494.9:c.257_259del	ENSP00000307101.5:p.Ala86_Arg87delinsGly
ENST00000361570.4:c.299_301del	ENSP00000355153.4:p.Ala100_Arg101delinsGl...
ENST00000380150.2:n.231_233del
ENST00000380151.3:c.531_533del	ENSP00000369496.3:n.531_533del
ENST00000404796.2:c.348-58333_348-58331del	ENSP00000385916.2:n.348-58333_348-58331de...
ENST00000479692.2:c.104_106del	ENSP00000466887.1:p.Ala35_Arg36delinsGly
ENST00000494262.5:c.104_106del	ENSP00000464952.1:p.Ala35_Arg36delinsGly
ENST00000497750.1:c.104_106del	ENSP00000468510.1:p.Ala35_Arg36delinsGly
ENST00000498124.1:c.257_259del	ENSP00000418915.1:p.Ala86_Arg87delinsGly
ENST00000498628.6:c.104_106del	ENSP00000467857.1:p.Ala35_Arg36delinsGly
ENST00000530628.2:c.300_302del	ENSP00000432664.2:p.Cys100_Pro101delinsTr...
ENST00000578845.2:c.104_106del	ENSP00000467390.1:p.Ala35_Arg36delinsGly
ENST00000579122.1:c.257_259del	ENSP00000464202.1:p.Ala86_Arg87delinsGly
ENST00000579755.1:c.300_302del	ENSP00000462950.1:p.Cys100_Pro101delinsTr...
NM_000077.4:c.257_259del , LRG_11t1:c.257_259del	NP_000068.1:p.Ala86_Arg87delinsGly
NM_001195132.1:c.257_259del	NP_001182061.1:p.Ala86_Arg87delinsGly
NM_058195.3:c.300_302del , LRG_11t2:c.300_302del	NP_478102.2:p.Cys100_Pro101delinsTrp
NM_058197.4:c.531_533del	NP_478104.2:n.531_533del
XM_005251343.1:c.104_106del	XP_005251400.1:p.Ala35_Arg36delinsGly
XM_011517675.1:c.257_259del	XP_011515977.1:p.Ala86_Arg87delinsGly
XM_011517676.1:c.257_259del	XP_011515978.1:p.Ala86_Arg87delinsGly
XM_011517679.1:c.104_106del	XP_011515981.1:p.Ala35_Arg36delinsGly
XR_929159.1:n.658_660del
XR_929161.1:n.447_449del
XR_929162.1:n.447_449del
XR_929163.1:n.396_398del
XR_929164.1:n.179_181del
NM_001363763.1:c.104_106del	NP_001350692.1:p.Ala35_Arg36delinsGly
XM_011517675.2:c.257_259del	XP_011515977.1:p.Ala86_Arg87delinsGly
XM_011517676.2:c.257_259del	XP_011515978.1:p.Ala86_Arg87delinsGly
XR_929159.2:n.587_589del
NM_001363763.2:c.104_106del	NP_001350692.1:p.Ala35_Arg36delinsGly
NM_000077.5:c.257_259del MANE Select	NP_000068.1:p.Ala86_Arg87delinsGly
NM_001195132.2:c.257_259del	NP_001182061.1:p.Ala86_Arg87delinsGly
NM_058195.4:c.300_302del MANE Plus Clinical	NP_478102.2:p.Cys100_Pro101delinsTrp
NM_058197.5:c.*180_*182del	NP_478104.2:n.*180_*182del