Canonical Allele Identifier: CA464261919

Gene: CDKN2A

Linked Data

• COSMIC: COSM231512 ; COSM231513 ; COSM231514
• MyVariant Identifiers: chr9:g.21971099del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971102del , CM000671.2:g.21971102del	GRCh38
NC_000009.11:g.21971101del , CM000671.1:g.21971101del	GRCh37
NC_000009.10:g.21961101del	NCBI36
NG_007485.1:g.28392del , LRG_11:g.28392del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.259del MANE Select	ENSP00000307101.5:p.Arg87GlyfsTer?
ENST00000404796.3:c.348-58331del	ENSP00000385916.2:n.348-58331del
ENST00000579755.2:c.302del MANE Plus Clinical	ENSP00000462950.1:p.Pro101ArgfsTer?
ENST00000304494.9:c.259del	ENSP00000307101.5:p.Arg87GlyfsTer?
ENST00000361570.4:c.301del	ENSP00000355153.4:p.Arg101GlyfsTer?
ENST00000380150.2:n.233del
ENST00000380151.3:c.533del	ENSP00000369496.3:n.533del
ENST00000404796.2:c.348-58331del	ENSP00000385916.2:n.348-58331del
ENST00000479692.2:c.106del	ENSP00000466887.1:p.Arg36GlyfsTer?
ENST00000494262.5:c.106del	ENSP00000464952.1:p.Arg36GlyfsTer?
ENST00000497750.1:c.106del	ENSP00000468510.1:p.Arg36GlyfsTer?
ENST00000498124.1:c.259del	ENSP00000418915.1:p.Arg87GlyfsTer?
ENST00000498628.6:c.106del	ENSP00000467857.1:p.Arg36GlyfsTer?
ENST00000530628.2:c.302del	ENSP00000432664.2:p.Pro101ArgfsTer?
ENST00000578845.2:c.106del	ENSP00000467390.1:p.Arg36GlyfsTer?
ENST00000579122.1:c.259del	ENSP00000464202.1:p.Arg87GlyfsTer?
ENST00000579755.1:c.302del	ENSP00000462950.1:p.Pro101ArgfsTer?
NM_000077.4:c.259del , LRG_11t1:c.259del	NP_000068.1:p.Arg87GlyfsTer?
NM_001195132.1:c.259del	NP_001182061.1:p.Arg87GlyfsTer?
NM_058195.3:c.302del , LRG_11t2:c.302del	NP_478102.2:p.Pro101ArgfsTer?
NM_058197.4:c.533del	NP_478104.2:n.533del
XM_005251343.1:c.106del	XP_005251400.1:p.Arg36GlyfsTer?
XM_011517675.1:c.259del	XP_011515977.1:p.Arg87GlyfsTer?
XM_011517676.1:c.259del	XP_011515978.1:p.Arg87GlyfsTer?
XM_011517679.1:c.106del	XP_011515981.1:p.Arg36GlyfsTer?
XR_929159.1:n.660del
XR_929161.1:n.449del
XR_929162.1:n.449del
XR_929163.1:n.398del
XR_929164.1:n.181del
NM_001363763.1:c.106del	NP_001350692.1:p.Arg36GlyfsTer?
XM_011517675.2:c.259del	XP_011515977.1:p.Arg87GlyfsTer?
XM_011517676.2:c.259del	XP_011515978.1:p.Arg87GlyfsTer?
XR_929159.2:n.589del
NM_001363763.2:c.106del	NP_001350692.1:p.Arg36GlyfsTer?
NM_000077.5:c.259del MANE Select	NP_000068.1:p.Arg87GlyfsTer?
NM_001195132.2:c.259del	NP_001182061.1:p.Arg87GlyfsTer?
NM_058195.4:c.302del MANE Plus Clinical	NP_478102.2:p.Pro101ArgfsTer?
NM_058197.5:c.*182del	NP_478104.2:n.*182del