Canonical Allele Identifier: CA645552471

Gene: CDKN2A

Linked Data

• COSMIC: COSM4387393

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971093_21971100del , CM000671.2:g.21971093_21971100del	GRCh38
NC_000009.11:g.21971092_21971099del , CM000671.1:g.21971092_21971099del	GRCh37
NC_000009.10:g.21961092_21961099del	NCBI36
NG_007485.1:g.28393_28400del , LRG_11:g.28393_28400del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.260_267del MANE Select	ENSP00000307101.5:p.Arg87LeufsTer30
ENST00000404796.3:c.348-58340_348-58333del	ENSP00000385916.2:n.348-58340_348-58333de...
ENST00000579755.2:c.303_310del MANE Plus Clinical	ENSP00000462950.1:p.Gly102SerfsTer?
ENST00000304494.9:c.260_267del	ENSP00000307101.5:p.Arg87LeufsTer30
ENST00000361570.4:c.302_309del	ENSP00000355153.4:p.Arg101LeufsTer30
ENST00000380150.2:n.234_241del
ENST00000380151.3:c.534_541del	ENSP00000369496.3:n.534_541del
ENST00000404796.2:c.348-58340_348-58333del	ENSP00000385916.2:n.348-58340_348-58333de...
ENST00000479692.2:c.107_114del	ENSP00000466887.1:p.Arg36LeufsTer30
ENST00000494262.5:c.107_114del	ENSP00000464952.1:p.Arg36LeufsTer30
ENST00000497750.1:c.107_114del	ENSP00000468510.1:p.Arg36LeufsTer30
ENST00000498124.1:c.260_267del	ENSP00000418915.1:p.Arg87LeufsTer30
ENST00000498628.6:c.107_114del	ENSP00000467857.1:p.Arg36LeufsTer30
ENST00000530628.2:c.303_310del	ENSP00000432664.2:p.Gly102SerfsTer?
ENST00000578845.2:c.107_114del	ENSP00000467390.1:p.Arg36LeufsTer30
ENST00000579122.1:c.260_267del	ENSP00000464202.1:p.Arg87LeufsTer30
ENST00000579755.1:c.303_310del	ENSP00000462950.1:p.Gly102SerfsTer?
NM_000077.4:c.260_267del , LRG_11t1:c.260_267del	NP_000068.1:p.Arg87LeufsTer30
NM_001195132.1:c.260_267del	NP_001182061.1:p.Arg87LeufsTer30
NM_058195.3:c.303_310del , LRG_11t2:c.303_310del	NP_478102.2:p.Gly102SerfsTer?
NM_058197.4:c.534_541del	NP_478104.2:n.534_541del
XM_005251343.1:c.107_114del	XP_005251400.1:p.Arg36LeufsTer30
XM_011517675.1:c.260_267del	XP_011515977.1:p.Arg87LeufsTer30
XM_011517676.1:c.260_267del	XP_011515978.1:p.Arg87LeufsTer30
XM_011517679.1:c.107_114del	XP_011515981.1:p.Arg36LeufsTer30
XR_929159.1:n.661_668del
XR_929161.1:n.450_457del
XR_929162.1:n.450_457del
XR_929163.1:n.399_406del
XR_929164.1:n.182_189del
NM_001363763.1:c.107_114del	NP_001350692.1:p.Arg36LeufsTer30
XM_011517675.2:c.260_267del	XP_011515977.1:p.Arg87LeufsTer30
XM_011517676.2:c.260_267del	XP_011515978.1:p.Arg87LeufsTer30
XR_929159.2:n.590_597del
NM_001363763.2:c.107_114del	NP_001350692.1:p.Arg36LeufsTer30
NM_000077.5:c.260_267del MANE Select	NP_000068.1:p.Arg87LeufsTer30
NM_001195132.2:c.260_267del	NP_001182061.1:p.Arg87LeufsTer30
NM_058195.4:c.303_310del MANE Plus Clinical	NP_478102.2:p.Gly102SerfsTer?
NM_058197.5:c.*183_*190del	NP_478104.2:n.*183_*190del