Canonical Allele Identifier: CA652685289

Gene: CDKN2A

Linked Data

• COSMIC: COSN25613393 ; COSN25613394

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968171_21968178del , CM000671.2:g.21968171_21968178del	GRCh38
NC_000009.11:g.21968170_21968177del , CM000671.1:g.21968170_21968177del	GRCh37
NC_000009.10:g.21958170_21958177del	NCBI36
NG_007485.1:g.31316_31323del , LRG_11:g.31316_31323del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*53_*60del MANE Select	ENSP00000307101.5:n.*53_*60del
ENST00000404796.3:c.348-61262_348-61255del	ENSP00000385916.2:n.348-61262_348-61255del
ENST00000579755.2:c.*168_*175del MANE Plus Clinical	ENSP00000462950.1:n.*168_*175del
ENST00000304494.9:c.*53_*60del	ENSP00000307101.5:n.*53_*60del
ENST00000361570.4:c.*53_*60del	ENSP00000355153.4:n.*53_*60del
ENST00000404796.2:c.348-61262_348-61255del	ENSP00000385916.2:n.348-61262_348-61255del
ENST00000498124.1:c.*217_*224del	ENSP00000418915.1:n.*217_*224del
ENST00000498628.6:c.*53_*60del	ENSP00000467857.1:n.*53_*60del
ENST00000530628.2:c.*94_*101del	ENSP00000432664.2:n.*94_*101del
ENST00000578845.2:c.*53_*60del	ENSP00000467390.1:n.*53_*60del
ENST00000579122.1:c.*33_*40del	ENSP00000464202.1:n.*33_*40del
ENST00000579755.1:c.*168_*175del	ENSP00000462950.1:n.*168_*175del
NM_000077.4:c.*53_*60del , LRG_11t1:c.*53_*60del	NP_000068.1:n.*53_*60del
NM_001195132.1:c.*217_*224del	NP_001182061.1:n.*217_*224del
NM_058195.3:c.*168_*175del , LRG_11t2:c.*168_*175del	NP_478102.2:n.*168_*175del
NM_058197.4:c.798_805del	NP_478104.2:n.798_805del
XM_005251343.1:c.*53_*60del	XP_005251400.1:n.*53_*60del
XM_011517679.1:c.*53_*60del	XP_011515981.1:n.*53_*60del
NM_001363763.1:c.*53_*60del	NP_001350692.1:n.*53_*60del
NM_001363763.2:c.*53_*60del	NP_001350692.1:n.*53_*60del
NM_000077.5:c.*53_*60del MANE Select	NP_000068.1:n.*53_*60del
NM_001195132.2:c.*217_*224del	NP_001182061.1:n.*217_*224del
NM_058195.4:c.*168_*175del MANE Plus Clinical	NP_478102.2:n.*168_*175del
NM_058197.5:c.*447_*454del	NP_478104.2:n.*447_*454del