Canonical Allele Identifier: CA645552501

Gene: CDKN2A

Linked Data

• COSMIC: COSM13524

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971121_21971122delinsAA , CM000671.2:g.21971121_21971122delinsAA	GRCh38
NC_000009.11:g.21971120_21971121delinsAA , CM000671.1:g.21971120_21971121delinsAA	GRCh37
NC_000009.10:g.21961120_21961121delinsAA	NCBI36
NG_007485.1:g.28370_28371delinsTT , LRG_11:g.28370_28371delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.237_238delinsTT MANE Select	ENSP00000307101.5:p.Thr80Ter
ENST00000404796.3:c.348-58312_348-58311delinsAA	ENSP00000385916.2:n.348-58312_348-58311delinsAA
ENST00000579755.2:c.280_281delinsTT MANE Plus Clinical	ENSP00000462950.1:p.Pro94Leu
ENST00000304494.9:c.237_238delinsTT	ENSP00000307101.5:p.Thr80Ter
ENST00000361570.4:c.280_281delinsTT	ENSP00000355153.4:p.Pro94Leu
ENST00000380150.2:n.211_212delinsTT
ENST00000380151.3:c.511_512delinsTT	ENSP00000369496.3:n.511_512delinsTT
ENST00000404796.2:c.348-58312_348-58311delinsAA	ENSP00000385916.2:n.348-58312_348-58311delinsAA
ENST00000479692.2:c.84_85delinsTT	ENSP00000466887.1:p.Thr29Ter
ENST00000494262.5:c.84_85delinsTT	ENSP00000464952.1:p.Thr29Ter
ENST00000497750.1:c.84_85delinsTT	ENSP00000468510.1:p.Thr29Ter
ENST00000498124.1:c.237_238delinsTT	ENSP00000418915.1:p.Thr80Ter
ENST00000498628.6:c.84_85delinsTT	ENSP00000467857.1:p.Thr29Ter
ENST00000530628.2:c.280_281delinsTT	ENSP00000432664.2:p.Pro94Leu
ENST00000578845.2:c.84_85delinsTT	ENSP00000467390.1:p.Thr29Ter
ENST00000579122.1:c.237_238delinsTT	ENSP00000464202.1:p.Thr80Ter
ENST00000579755.1:c.280_281delinsTT	ENSP00000462950.1:p.Pro94Leu
NM_000077.4:c.237_238delinsTT , LRG_11t1:c.237_238delinsTT	NP_000068.1:p.Thr80Ter
NM_001195132.1:c.237_238delinsTT	NP_001182061.1:p.Thr80Ter
NM_058195.3:c.280_281delinsTT , LRG_11t2:c.280_281delinsTT	NP_478102.2:p.Pro94Leu
NM_058197.4:c.511_512delinsTT	NP_478104.2:n.511_512delinsTT
XM_005251343.1:c.84_85delinsTT	XP_005251400.1:p.Thr29Ter
XM_011517675.1:c.237_238delinsTT	XP_011515977.1:p.Thr80Ter
XM_011517676.1:c.237_238delinsTT	XP_011515978.1:p.Thr80Ter
XM_011517679.1:c.84_85delinsTT	XP_011515981.1:p.Thr29Ter
XR_929159.1:n.638_639delinsTT
XR_929161.1:n.427_428delinsTT
XR_929162.1:n.427_428delinsTT
XR_929163.1:n.376_377delinsTT
XR_929164.1:n.159_160delinsTT
NM_001363763.1:c.84_85delinsTT	NP_001350692.1:p.Thr29Ter
XM_011517675.2:c.237_238delinsTT	XP_011515977.1:p.Thr80Ter
XM_011517676.2:c.237_238delinsTT	XP_011515978.1:p.Thr80Ter
XR_929159.2:n.567_568delinsTT
NM_001363763.2:c.84_85delinsTT	NP_001350692.1:p.Thr29Ter
NM_000077.5:c.237_238delinsTT MANE Select	NP_000068.1:p.Thr80Ter
NM_001195132.2:c.237_238delinsTT	NP_001182061.1:p.Thr80Ter
NM_058195.4:c.280_281delinsTT MANE Plus Clinical	NP_478102.2:p.Pro94Leu
NM_058197.5:c.*160_*161delinsTT	NP_478104.2:n.*160_*161delinsTT