Canonical Allele Identifier: CA645552420

Gene: CDKN2A

Linked Data

• COSMIC: COSM4387394

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21970919del , CM000671.2:g.21970919del	GRCh38
NC_000009.11:g.21970918del , CM000671.1:g.21970918del	GRCh37
NC_000009.10:g.21960918del	NCBI36
NG_007485.1:g.28574del , LRG_11:g.28574del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.441del MANE Select	ENSP00000307101.5:p.Ala148ArgfsTer?
ENST00000404796.3:c.348-58514del	ENSP00000385916.2:n.348-58514del
ENST00000579755.2:c.*85del MANE Plus Clinical	ENSP00000462950.1:n.*85del
ENST00000304494.9:c.441del	ENSP00000307101.5:p.Ala148ArgfsTer?
ENST00000361570.4:c.483del	ENSP00000355153.4:p.Ala162ArgfsTer?
ENST00000380150.2:n.415del
ENST00000380151.3:c.715del	ENSP00000369496.3:n.715del
ENST00000404796.2:c.348-58514del	ENSP00000385916.2:n.348-58514del
ENST00000479692.2:c.288del	ENSP00000466887.1:p.Ala97ArgfsTer?
ENST00000494262.5:c.288del	ENSP00000464952.1:p.Ala97ArgfsTer?
ENST00000497750.1:c.288del	ENSP00000468510.1:p.Ala97ArgfsTer?
ENST00000498124.1:c.441del	ENSP00000418915.1:p.Ala148ArgfsTer7
ENST00000498628.6:c.288del	ENSP00000467857.1:p.Ala97ArgfsTer?
ENST00000530628.2:c.*27+58del	ENSP00000432664.2:n.*27+58del
ENST00000578845.2:c.288del	ENSP00000467390.1:p.Ala97ArgfsTer?
ENST00000579122.1:c.383+58del	ENSP00000464202.1:n.383+58del
ENST00000579755.1:c.*85del	ENSP00000462950.1:n.*85del
NM_000077.4:c.441del , LRG_11t1:c.441del	NP_000068.1:p.Ala148ArgfsTer?
NM_001195132.1:c.441del	NP_001182061.1:p.Ala148ArgfsTer7
NM_058195.3:c.*85del , LRG_11t2:c.*85del	NP_478102.2:n.*85del
NM_058197.4:c.715del	NP_478104.2:n.715del
XM_005251343.1:c.288del	XP_005251400.1:p.Ala97ArgfsTer?
XM_011517675.1:c.441del	XP_011515977.1:p.Ala148ArgfsTer?
XM_011517676.1:c.441del	XP_011515978.1:p.Ala148ArgfsTer?
XM_011517679.1:c.288del	XP_011515981.1:p.Ala97ArgfsTer?
XR_929159.1:n.842del
XR_929161.1:n.631del
XR_929162.1:n.631del
XR_929163.1:n.580del
XR_929164.1:n.363del
NM_001363763.1:c.288del	NP_001350692.1:p.Ala97ArgfsTer?
XM_011517675.2:c.441del	XP_011515977.1:p.Ala148ArgfsTer?
XM_011517676.2:c.441del	XP_011515978.1:p.Ala148ArgfsTer?
XR_929159.2:n.771del
NM_001363763.2:c.288del	NP_001350692.1:p.Ala97ArgfsTer?
NM_000077.5:c.441del MANE Select	NP_000068.1:p.Ala148ArgfsTer?
NM_001195132.2:c.441del	NP_001182061.1:p.Ala148ArgfsTer7
NM_058195.4:c.*85del MANE Plus Clinical	NP_478102.2:n.*85del
NM_058197.5:c.*364del	NP_478104.2:n.*364del