Canonical Allele Identifier: CA645552549

Gene: CDKN2A

Linked Data

• COSMIC: COSM13762

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971178_21971190del , CM000671.2:g.21971178_21971190del	GRCh38
NC_000009.11:g.21971177_21971189del , CM000671.1:g.21971177_21971189del	GRCh37
NC_000009.10:g.21961177_21961189del	NCBI36
NG_007485.1:g.28302_28314del , LRG_11:g.28302_28314del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.169_181del MANE Select	ENSP00000307101.5:p.Ala57SerfsTer?
ENST00000404796.3:c.348-58255_348-58243del	ENSP00000385916.2:n.348-58255_348-58243de...
ENST00000579755.2:c.212_224del MANE Plus Clinical	ENSP00000462950.1:p.Arg71GlnfsTer?
ENST00000304494.9:c.169_181del	ENSP00000307101.5:p.Ala57SerfsTer?
ENST00000361570.4:c.212_224del	ENSP00000355153.4:p.Arg71GlnfsTer?
ENST00000380150.2:n.143_155del
ENST00000380151.3:c.443_455del	ENSP00000369496.3:n.443_455del
ENST00000404796.2:c.348-58255_348-58243del	ENSP00000385916.2:n.348-58255_348-58243de...
ENST00000479692.2:c.16_28del	ENSP00000466887.1:p.Ala6SerfsTer?
ENST00000494262.5:c.16_28del	ENSP00000464952.1:p.Ala6SerfsTer?
ENST00000497750.1:c.16_28del	ENSP00000468510.1:p.Ala6SerfsTer?
ENST00000498124.1:c.169_181del	ENSP00000418915.1:p.Ala57SerfsTer?
ENST00000498628.6:c.16_28del	ENSP00000467857.1:p.Ala6SerfsTer?
ENST00000530628.2:c.212_224del	ENSP00000432664.2:p.Arg71GlnfsTer?
ENST00000578845.2:c.16_28del	ENSP00000467390.1:p.Ala6SerfsTer?
ENST00000579122.1:c.169_181del	ENSP00000464202.1:p.Ala57SerfsTer?
ENST00000579755.1:c.212_224del	ENSP00000462950.1:p.Arg71GlnfsTer?
NM_000077.4:c.169_181del , LRG_11t1:c.169_181del	NP_000068.1:p.Ala57SerfsTer?
NM_001195132.1:c.169_181del	NP_001182061.1:p.Ala57SerfsTer?
NM_058195.3:c.212_224del , LRG_11t2:c.212_224del	NP_478102.2:p.Arg71GlnfsTer?
NM_058197.4:c.443_455del	NP_478104.2:n.443_455del
XM_005251343.1:c.16_28del	XP_005251400.1:p.Ala6SerfsTer?
XM_011517675.1:c.169_181del	XP_011515977.1:p.Ala57SerfsTer?
XM_011517676.1:c.169_181del	XP_011515978.1:p.Ala57SerfsTer?
XM_011517679.1:c.16_28del	XP_011515981.1:p.Ala6SerfsTer?
XR_929159.1:n.570_582del
XR_929161.1:n.359_371del
XR_929162.1:n.359_371del
XR_929163.1:n.308_320del
XR_929164.1:n.91_103del
NM_001363763.1:c.16_28del	NP_001350692.1:p.Ala6SerfsTer?
XM_011517675.2:c.169_181del	XP_011515977.1:p.Ala57SerfsTer?
XM_011517676.2:c.169_181del	XP_011515978.1:p.Ala57SerfsTer?
XR_929159.2:n.499_511del
NM_001363763.2:c.16_28del	NP_001350692.1:p.Ala6SerfsTer?
NM_000077.5:c.169_181del MANE Select	NP_000068.1:p.Ala57SerfsTer?
NM_001195132.2:c.169_181del	NP_001182061.1:p.Ala57SerfsTer?
NM_058195.4:c.212_224del MANE Plus Clinical	NP_478102.2:p.Arg71GlnfsTer?
NM_058197.5:c.*92_*104del	NP_478104.2:n.*92_*104del