Canonical Allele Identifier: CA645552446

Gene: CDKN2A

Linked Data

• COSMIC: COSM85566

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971026_21971044del , CM000671.2:g.21971026_21971044del	GRCh38
NC_000009.11:g.21971025_21971043del , CM000671.1:g.21971025_21971043del	GRCh37
NC_000009.10:g.21961025_21961043del	NCBI36
NG_007485.1:g.28451_28469del , LRG_11:g.28451_28469del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.318_336del MANE Select	ENSP00000307101.5:p.Arg107CysfsTer?
ENST00000404796.3:c.348-58407_348-58389del	ENSP00000385916.2:n.348-58407_348-58389de...
ENST00000579755.2:c.361_379del MANE Plus Clinical	ENSP00000462950.1:p.Ala121LeufsTer?
ENST00000304494.9:c.318_336del	ENSP00000307101.5:p.Arg107CysfsTer?
ENST00000361570.4:c.360_378del	ENSP00000355153.4:p.Arg121CysfsTer?
ENST00000380150.2:n.292_310del
ENST00000380151.3:c.592_610del	ENSP00000369496.3:n.592_610del
ENST00000404796.2:c.348-58407_348-58389del	ENSP00000385916.2:n.348-58407_348-58389de...
ENST00000479692.2:c.165_183del	ENSP00000466887.1:p.Arg56CysfsTer?
ENST00000494262.5:c.165_183del	ENSP00000464952.1:p.Arg56CysfsTer?
ENST00000497750.1:c.165_183del	ENSP00000468510.1:p.Arg56CysfsTer?
ENST00000498124.1:c.318_336del	ENSP00000418915.1:p.Arg107CysfsTer?
ENST00000498628.6:c.165_183del	ENSP00000467857.1:p.Arg56CysfsTer?
ENST00000530628.2:c.361_379del	ENSP00000432664.2:p.Ala121LeufsTer27
ENST00000578845.2:c.165_183del	ENSP00000467390.1:p.Arg56CysfsTer?
ENST00000579122.1:c.318_336del	ENSP00000464202.1:p.Arg107CysfsTer20
ENST00000579755.1:c.361_379del	ENSP00000462950.1:p.Ala121LeufsTer?
NM_000077.4:c.318_336del , LRG_11t1:c.318_336del	NP_000068.1:p.Arg107CysfsTer?
NM_001195132.1:c.318_336del	NP_001182061.1:p.Arg107CysfsTer?
NM_058195.3:c.361_379del , LRG_11t2:c.361_379del	NP_478102.2:p.Ala121LeufsTer?
NM_058197.4:c.592_610del	NP_478104.2:n.592_610del
XM_005251343.1:c.165_183del	XP_005251400.1:p.Arg56CysfsTer?
XM_011517675.1:c.318_336del	XP_011515977.1:p.Arg107CysfsTer?
XM_011517676.1:c.318_336del	XP_011515978.1:p.Arg107CysfsTer?
XM_011517679.1:c.165_183del	XP_011515981.1:p.Arg56CysfsTer?
XR_929159.1:n.719_737del
XR_929161.1:n.508_526del
XR_929162.1:n.508_526del
XR_929163.1:n.457_475del
XR_929164.1:n.240_258del
NM_001363763.1:c.165_183del	NP_001350692.1:p.Arg56CysfsTer?
XM_011517675.2:c.318_336del	XP_011515977.1:p.Arg107CysfsTer?
XM_011517676.2:c.318_336del	XP_011515978.1:p.Arg107CysfsTer?
XR_929159.2:n.648_666del
NM_001363763.2:c.165_183del	NP_001350692.1:p.Arg56CysfsTer?
NM_000077.5:c.318_336del MANE Select	NP_000068.1:p.Arg107CysfsTer?
NM_001195132.2:c.318_336del	NP_001182061.1:p.Arg107CysfsTer?
NM_058195.4:c.361_379del MANE Plus Clinical	NP_478102.2:p.Ala121LeufsTer?
NM_058197.5:c.*241_*259del	NP_478104.2:n.*241_*259del