Canonical Allele Identifier: CA645552418

Gene: CDKN2A

Linked Data

• COSMIC: COSM5751686 ; COSM5751687 ; COSM5751688

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21970900_21970901insT , CM000671.2:g.21970900_21970901insT	GRCh38
NC_000009.11:g.21970899_21970900insT , CM000671.1:g.21970899_21970900insT	GRCh37
NC_000009.10:g.21960899_21960900insT	NCBI36
NG_007485.1:g.28591_28592insA , LRG_11:g.28591_28592insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.457+1_457+2insA MANE Select	ENSP00000307101.5:n.457+1_457+2insA
ENST00000404796.3:c.348-58533_348-58532insT	ENSP00000385916.2:n.348-58533_348-58532in...
ENST00000579755.2:c.*101+1_*101+2insA MANE Plus Clinical	ENSP00000462950.1:n.*101+1_*101+2insA
ENST00000304494.9:c.457+1_457+2insA	ENSP00000307101.5:n.457+1_457+2insA
ENST00000361570.4:c.499+1_499+2insA	ENSP00000355153.4:n.499+1_499+2insA
ENST00000380150.2:n.431+1_431+2insA
ENST00000380151.3:c.731+1_731+2insA	ENSP00000369496.3:n.731+1_731+2insA
ENST00000404796.2:c.348-58533_348-58532insT	ENSP00000385916.2:n.348-58533_348-58532in...
ENST00000479692.2:c.304+1_304+2insA	ENSP00000466887.1:n.304+1_304+2insA
ENST00000494262.5:c.304+1_304+2insA	ENSP00000464952.1:n.304+1_304+2insA
ENST00000497750.1:c.305_306insA	ENSP00000468510.1:p.Glu103Ter
ENST00000498124.1:c.457+1_457+2insA	ENSP00000418915.1:n.457+1_457+2insA
ENST00000498628.6:c.304+1_304+2insA	ENSP00000467857.1:n.304+1_304+2insA
ENST00000530628.2:c.*27+75_*27+76insA	ENSP00000432664.2:n.*27+75_*27+76insA
ENST00000578845.2:c.304+1_304+2insA	ENSP00000467390.1:n.304+1_304+2insA
ENST00000579122.1:c.383+75_383+76insA	ENSP00000464202.1:n.383+75_383+76insA
ENST00000579755.1:c.*101+1_*101+2insA	ENSP00000462950.1:n.*101+1_*101+2insA
NM_000077.4:c.457+1_457+2insA , LRG_11t1:c.457+1_457+2insA	NP_000068.1:n.457+1_457+2insA
NM_001195132.1:c.457+1_457+2insA	NP_001182061.1:n.457+1_457+2insA
NM_058195.3:c.*101+1_*101+2insA , LRG_11t2:c.*101+1_*101+2insA	NP_478102.2:n.*101+1_*101+2insA
NM_058197.4:c.731+1_731+2insA	NP_478104.2:n.731+1_731+2insA
XM_005251343.1:c.304+1_304+2insA	XP_005251400.1:n.304+1_304+2insA
XM_011517675.1:c.457+1_457+2insA	XP_011515977.1:n.457+1_457+2insA
XM_011517676.1:c.457+1_457+2insA	XP_011515978.1:n.457+1_457+2insA
XM_011517679.1:c.304+1_304+2insA	XP_011515981.1:n.304+1_304+2insA
XR_929159.1:n.858+1_858+2insA
XR_929161.1:n.647+1_647+2insA
XR_929162.1:n.647+1_647+2insA
XR_929163.1:n.596+1_596+2insA
XR_929164.1:n.379+1_379+2insA
NM_001363763.1:c.304+1_304+2insA	NP_001350692.1:n.304+1_304+2insA
XM_011517675.2:c.457+1_457+2insA	XP_011515977.1:n.457+1_457+2insA
XM_011517676.2:c.457+1_457+2insA	XP_011515978.1:n.457+1_457+2insA
XR_929159.2:n.787+1_787+2insA
NM_001363763.2:c.304+1_304+2insA	NP_001350692.1:n.304+1_304+2insA
NM_000077.5:c.457+1_457+2insA MANE Select	NP_000068.1:n.457+1_457+2insA
NM_001195132.2:c.457+1_457+2insA	NP_001182061.1:n.457+1_457+2insA
NM_058195.4:c.*101+1_*101+2insA MANE Plus Clinical	NP_478102.2:n.*101+1_*101+2insA
NM_058197.5:c.*380+1_*380+2insA	NP_478104.2:n.*380+1_*380+2insA