Canonical Allele Identifier: CA645552482

Gene: CDKN2A

Linked Data

• COSMIC: COSM13297

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971109_21971110insAA , CM000671.2:g.21971109_21971110insAA	GRCh38
NC_000009.11:g.21971108_21971109insAA , CM000671.1:g.21971108_21971109insAA	GRCh37
NC_000009.10:g.21961108_21961109insAA	NCBI36
NG_007485.1:g.28382_28383insTT , LRG_11:g.28382_28383insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.249_250insTT MANE Select	ENSP00000307101.5:p.Asp84LeufsTer?
ENST00000404796.3:c.348-58324_348-58323insAA	ENSP00000385916.2:n.348-58324_348-58323insAA
ENST00000579755.2:c.292_293insTT MANE Plus Clinical	ENSP00000462950.1:p.Arg98LeufsTer?
ENST00000304494.9:c.249_250insTT	ENSP00000307101.5:p.Asp84LeufsTer?
ENST00000361570.4:c.291_292insTT	ENSP00000355153.4:p.Asp98LeufsTer?
ENST00000380150.2:n.223_224insTT
ENST00000380151.3:c.523_524insTT	ENSP00000369496.3:n.523_524insTT
ENST00000404796.2:c.348-58324_348-58323insAA	ENSP00000385916.2:n.348-58324_348-58323insAA
ENST00000479692.2:c.96_97insTT	ENSP00000466887.1:p.Asp33LeufsTer?
ENST00000494262.5:c.96_97insTT	ENSP00000464952.1:p.Asp33LeufsTer?
ENST00000497750.1:c.96_97insTT	ENSP00000468510.1:p.Asp33LeufsTer?
ENST00000498124.1:c.249_250insTT	ENSP00000418915.1:p.Asp84LeufsTer?
ENST00000498628.6:c.96_97insTT	ENSP00000467857.1:p.Asp33LeufsTer?
ENST00000530628.2:c.292_293insTT	ENSP00000432664.2:p.Arg98LeufsTer?
ENST00000578845.2:c.96_97insTT	ENSP00000467390.1:p.Asp33LeufsTer?
ENST00000579122.1:c.249_250insTT	ENSP00000464202.1:p.Asp84LeufsTer?
ENST00000579755.1:c.292_293insTT	ENSP00000462950.1:p.Arg98LeufsTer?
NM_000077.4:c.249_250insTT , LRG_11t1:c.249_250insTT	NP_000068.1:p.Asp84LeufsTer?
NM_001195132.1:c.249_250insTT	NP_001182061.1:p.Asp84LeufsTer?
NM_058195.3:c.292_293insTT , LRG_11t2:c.292_293insTT	NP_478102.2:p.Arg98LeufsTer?
NM_058197.4:c.523_524insTT	NP_478104.2:n.523_524insTT
XM_005251343.1:c.96_97insTT	XP_005251400.1:p.Asp33LeufsTer?
XM_011517675.1:c.249_250insTT	XP_011515977.1:p.Asp84LeufsTer?
XM_011517676.1:c.249_250insTT	XP_011515978.1:p.Asp84LeufsTer?
XM_011517679.1:c.96_97insTT	XP_011515981.1:p.Asp33LeufsTer?
XR_929159.1:n.650_651insTT
XR_929161.1:n.439_440insTT
XR_929162.1:n.439_440insTT
XR_929163.1:n.388_389insTT
XR_929164.1:n.171_172insTT
NM_001363763.1:c.96_97insTT	NP_001350692.1:p.Asp33LeufsTer?
XM_011517675.2:c.249_250insTT	XP_011515977.1:p.Asp84LeufsTer?
XM_011517676.2:c.249_250insTT	XP_011515978.1:p.Asp84LeufsTer?
XR_929159.2:n.579_580insTT
NM_001363763.2:c.96_97insTT	NP_001350692.1:p.Asp33LeufsTer?
NM_000077.5:c.249_250insTT MANE Select	NP_000068.1:p.Asp84LeufsTer?
NM_001195132.2:c.249_250insTT	NP_001182061.1:p.Asp84LeufsTer?
NM_058195.4:c.292_293insTT MANE Plus Clinical	NP_478102.2:p.Arg98LeufsTer?
NM_058197.5:c.*172_*173insTT	NP_478104.2:n.*172_*173insTT