Canonical Allele Identifier: CA1139660895

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1819678649

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21970895_21970897delinsACA , CM000671.2:g.21970895_21970897delinsACA	GRCh38
NC_000009.11:g.21970894_21970896delinsACA , CM000671.1:g.21970894_21970896delinsACA	GRCh37
NC_000009.10:g.21960894_21960896delinsACA	NCBI36
NG_007485.1:g.28595_28597delinsTGT , LRG_11:g.28595_28597delinsTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.457+5_457+7delinsTGT MANE Select	ENSP00000307101.5:n.457+5_457+7delinsTGT
ENST00000404796.3:c.348-58538_348-58536delinsACA	ENSP00000385916.2:n.348-58538_348-58536de...
ENST00000579755.2:c.*101+5_*101+7delinsTGT MANE Plus Clinical	ENSP00000462950.1:n.*101+5_*101+7delinsTG...
ENST00000304494.9:c.457+5_457+7delinsTGT	ENSP00000307101.5:n.457+5_457+7delinsTGT
ENST00000361570.4:c.499+5_499+7delinsTGT	ENSP00000355153.4:n.499+5_499+7delinsTGT
ENST00000380150.2:n.431+5_431+7delinsTGT
ENST00000380151.3:c.731+5_731+7delinsTGT	ENSP00000369496.3:n.731+5_731+7delinsTGT
ENST00000404796.2:c.348-58538_348-58536delinsACA	ENSP00000385916.2:n.348-58538_348-58536de...
ENST00000479692.2:c.304+5_304+7delinsTGT	ENSP00000466887.1:n.304+5_304+7delinsTGT
ENST00000494262.5:c.304+5_304+7delinsTGT	ENSP00000464952.1:n.304+5_304+7delinsTGT
ENST00000497750.1:c.309_311delinsTGT	ENSP00000468510.1:p.Glu103_Asp104delinsAs...
ENST00000498124.1:c.457+5_457+7delinsTGT	ENSP00000418915.1:n.457+5_457+7delinsTGT
ENST00000498628.6:c.304+5_304+7delinsTGT	ENSP00000467857.1:n.304+5_304+7delinsTGT
ENST00000530628.2:c.*27+79_*27+81delinsTGT	ENSP00000432664.2:n.*27+79_*27+81delinsTG...
ENST00000578845.2:c.304+5_304+7delinsTGT	ENSP00000467390.1:n.304+5_304+7delinsTGT
ENST00000579122.1:c.383+79_383+81delinsTGT	ENSP00000464202.1:n.383+79_383+81delinsTG...
ENST00000579755.1:c.*101+5_*101+7delinsTGT	ENSP00000462950.1:n.*101+5_*101+7delinsTG...
NM_000077.4:c.457+5_457+7delinsTGT , LRG_11t1:c.457+5_457+7delinsTGT	NP_000068.1:n.457+5_457+7delinsTGT
NM_001195132.1:c.457+5_457+7delinsTGT	NP_001182061.1:n.457+5_457+7delinsTGT
NM_058195.3:c.*101+5_*101+7delinsTGT , LRG_11t2:c.*101+5_*101+7delinsTGT	NP_478102.2:n.*101+5_*101+7delinsTGT
NM_058197.4:c.731+5_731+7delinsTGT	NP_478104.2:n.731+5_731+7delinsTGT
XM_005251343.1:c.304+5_304+7delinsTGT	XP_005251400.1:n.304+5_304+7delinsTGT
XM_011517675.1:c.457+5_457+7delinsTGT	XP_011515977.1:n.457+5_457+7delinsTGT
XM_011517676.1:c.457+5_457+7delinsTGT	XP_011515978.1:n.457+5_457+7delinsTGT
XM_011517679.1:c.304+5_304+7delinsTGT	XP_011515981.1:n.304+5_304+7delinsTGT
XR_929159.1:n.858+5_858+7delinsTGT
XR_929161.1:n.647+5_647+7delinsTGT
XR_929162.1:n.647+5_647+7delinsTGT
XR_929163.1:n.596+5_596+7delinsTGT
XR_929164.1:n.379+5_379+7delinsTGT
NM_001363763.1:c.304+5_304+7delinsTGT	NP_001350692.1:n.304+5_304+7delinsTGT
XM_011517675.2:c.457+5_457+7delinsTGT	XP_011515977.1:n.457+5_457+7delinsTGT
XM_011517676.2:c.457+5_457+7delinsTGT	XP_011515978.1:n.457+5_457+7delinsTGT
XR_929159.2:n.787+5_787+7delinsTGT
NM_001363763.2:c.304+5_304+7delinsTGT	NP_001350692.1:n.304+5_304+7delinsTGT
NM_000077.5:c.457+5_457+7delinsTGT MANE Select	NP_000068.1:n.457+5_457+7delinsTGT
NM_001195132.2:c.457+5_457+7delinsTGT	NP_001182061.1:n.457+5_457+7delinsTGT
NM_058195.4:c.*101+5_*101+7delinsTGT MANE Plus Clinical	NP_478102.2:n.*101+5_*101+7delinsTGT
NM_058197.5:c.*380+5_*380+7delinsTGT	NP_478104.2:n.*380+5_*380+7delinsTGT