Canonical Allele Identifier: CA645552419

Gene: CDKN2A

Linked Data

• COSMIC: COSM5876074 ; COSM5876075 ; COSM5876076

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21970916del , CM000671.2:g.21970916del	GRCh38
NC_000009.11:g.21970915del , CM000671.1:g.21970915del	GRCh37
NC_000009.10:g.21960915del	NCBI36
NG_007485.1:g.28576del , LRG_11:g.28576del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.443del MANE Select	ENSP00000307101.5:p.Ala148GlyfsTer?
ENST00000404796.3:c.348-58517del	ENSP00000385916.2:n.348-58517del
ENST00000579755.2:c.*87del MANE Plus Clinical	ENSP00000462950.1:n.*87del
ENST00000304494.9:c.443del	ENSP00000307101.5:p.Ala148GlyfsTer?
ENST00000361570.4:c.485del	ENSP00000355153.4:p.Ala162GlyfsTer?
ENST00000380150.2:n.417del
ENST00000380151.3:c.717del	ENSP00000369496.3:n.717del
ENST00000404796.2:c.348-58517del	ENSP00000385916.2:n.348-58517del
ENST00000479692.2:c.290del	ENSP00000466887.1:p.Ala97GlyfsTer?
ENST00000494262.5:c.290del	ENSP00000464952.1:p.Ala97GlyfsTer?
ENST00000497750.1:c.290del	ENSP00000468510.1:p.Ala97GlyfsTer?
ENST00000498124.1:c.443del	ENSP00000418915.1:p.Ala148GlyfsTer7
ENST00000498628.6:c.290del	ENSP00000467857.1:p.Ala97GlyfsTer?
ENST00000530628.2:c.*27+60del	ENSP00000432664.2:n.*27+60del
ENST00000578845.2:c.290del	ENSP00000467390.1:p.Ala97GlyfsTer?
ENST00000579122.1:c.383+60del	ENSP00000464202.1:n.383+60del
ENST00000579755.1:c.*87del	ENSP00000462950.1:n.*87del
NM_000077.4:c.443del , LRG_11t1:c.443del	NP_000068.1:p.Ala148GlyfsTer?
NM_001195132.1:c.443del	NP_001182061.1:p.Ala148GlyfsTer7
NM_058195.3:c.*87del , LRG_11t2:c.*87del	NP_478102.2:n.*87del
NM_058197.4:c.717del	NP_478104.2:n.717del
XM_005251343.1:c.290del	XP_005251400.1:p.Ala97GlyfsTer?
XM_011517675.1:c.443del	XP_011515977.1:p.Ala148GlyfsTer?
XM_011517676.1:c.443del	XP_011515978.1:p.Ala148GlyfsTer?
XM_011517679.1:c.290del	XP_011515981.1:p.Ala97GlyfsTer?
XR_929159.1:n.844del
XR_929161.1:n.633del
XR_929162.1:n.633del
XR_929163.1:n.582del
XR_929164.1:n.365del
NM_001363763.1:c.290del	NP_001350692.1:p.Ala97GlyfsTer?
XM_011517675.2:c.443del	XP_011515977.1:p.Ala148GlyfsTer?
XM_011517676.2:c.443del	XP_011515978.1:p.Ala148GlyfsTer?
XR_929159.2:n.773del
NM_001363763.2:c.290del	NP_001350692.1:p.Ala97GlyfsTer?
NM_000077.5:c.443del MANE Select	NP_000068.1:p.Ala148GlyfsTer?
NM_001195132.2:c.443del	NP_001182061.1:p.Ala148GlyfsTer7
NM_058195.4:c.*87del MANE Plus Clinical	NP_478102.2:n.*87del
NM_058197.5:c.*366del	NP_478104.2:n.*366del