Canonical Allele Identifier: CA645552591

Gene: CDKN2A

Linked Data

• COSMIC: COSM13718

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974666_21974698del , CM000671.2:g.21974666_21974698del	GRCh38
NC_000009.11:g.21974665_21974697del , CM000671.1:g.21974665_21974697del	GRCh37
NC_000009.10:g.21964665_21964697del	NCBI36
NG_007485.1:g.24795_24827del , LRG_11:g.24795_24827del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.131_150+13del
ENST00000404796.3:c.348-54767_348-54735del	ENSP00000385916.2:n.348-54767_348-54735de...
ENST00000579755.2:c.194-3489_194-3457del MANE Plus Clinical	ENSP00000462950.1:n.194-3489_194-3457del
ENST00000304494.9:c.131_150+13del
ENST00000361570.4:c.194-3489_194-3457del	ENSP00000355153.4:n.194-3489_194-3457del
ENST00000380151.3:c.131_163del	ENSP00000369496.3:p.Tyr44_Gly54del
ENST00000404796.2:c.348-54767_348-54735del	ENSP00000385916.2:n.348-54767_348-54735de...
ENST00000494262.5:c.-3-3489_-3-3457del	ENSP00000464952.1:n.-3-3489_-3-3457del
ENST00000498124.1:c.131_150+13del
ENST00000498628.6:c.-3-3489_-3-3457del	ENSP00000467857.1:n.-3-3489_-3-3457del
ENST00000530628.2:c.194-3489_194-3457del	ENSP00000432664.2:n.194-3489_194-3457del
ENST00000579122.1:c.131_150+13del
ENST00000579755.1:c.194-3489_194-3457del	ENSP00000462950.1:n.194-3489_194-3457del
NM_000077.4:c.131_150+13del , LRG_11t1:c.131_150+13del
NM_001195132.1:c.131_150+13del
NM_058195.3:c.194-3489_194-3457del , LRG_11t2:c.194-3489_194-3457del	NP_478102.2:n.194-3489_194-3457del
NM_058197.4:c.131_163del	NP_478104.2:p.Tyr44_Gly54del
XM_011517675.1:c.131_150+13del
XM_011517676.1:c.131_150+13del
XM_011517679.1:c.-3-3489_-3-3457del	XP_011515981.1:n.-3-3489_-3-3457del
XR_929159.1:n.532_551+13del
XR_929161.1:n.341-3489_341-3457del
XR_929162.1:n.341-3489_341-3457del
XR_929163.1:n.290-3489_290-3457del
NM_001363763.1:c.-3-3489_-3-3457del	NP_001350692.1:n.-3-3489_-3-3457del
XM_011517675.2:c.131_150+13del
XM_011517676.2:c.131_150+13del
XR_929159.2:n.461_480+13del
NM_001363763.2:c.-3-3489_-3-3457del	NP_001350692.1:n.-3-3489_-3-3457del
NM_000077.5:c.131_150+13del
NM_001195132.2:c.131_150+13del
NM_058195.4:c.194-3489_194-3457del MANE Plus Clinical	NP_478102.2:n.194-3489_194-3457del
NM_058197.5:c.131_163del	NP_478104.2:p.Tyr44_Gly54del