Canonical Allele Identifier: CA645552467

Gene: CDKN2A

Linked Data

• COSMIC: COSM28568

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971078_21971179del , CM000671.2:g.21971078_21971179del	GRCh38
NC_000009.11:g.21971077_21971178del , CM000671.1:g.21971077_21971178del	GRCh37
NC_000009.10:g.21961077_21961178del	NCBI36
NG_007485.1:g.28315_28416del , LRG_11:g.28315_28416del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.182_283del MANE Select	ENSP00000307101.5:p.Glu61_Leu94del
ENST00000404796.3:c.348-58355_348-58254del	ENSP00000385916.2:n.348-58355_348-58254de...
ENST00000579755.2:c.225_326del MANE Plus Clinical	ENSP00000462950.1:p.Ala76_Gly109del
ENST00000304494.9:c.182_283del	ENSP00000307101.5:p.Glu61_Leu94del
ENST00000361570.4:c.225_325del
ENST00000380150.2:n.156_257del
ENST00000380151.3:c.456_557del	ENSP00000369496.3:n.456_557del
ENST00000404796.2:c.348-58355_348-58254del	ENSP00000385916.2:n.348-58355_348-58254de...
ENST00000479692.2:c.29_130del	ENSP00000466887.1:p.Glu10_Leu43del
ENST00000494262.5:c.29_130del	ENSP00000464952.1:p.Glu10_Leu43del
ENST00000497750.1:c.29_130del	ENSP00000468510.1:p.Glu10_Leu43del
ENST00000498124.1:c.182_283del	ENSP00000418915.1:p.Glu61_Leu94del
ENST00000498628.6:c.29_130del	ENSP00000467857.1:p.Glu10_Leu43del
ENST00000530628.2:c.225_326del	ENSP00000432664.2:p.Ala76_Gly109del
ENST00000578845.2:c.29_130del	ENSP00000467390.1:p.Glu10_Leu43del
ENST00000579122.1:c.182_283del	ENSP00000464202.1:p.Glu61_Leu94del
ENST00000579755.1:c.225_326del	ENSP00000462950.1:p.Ala76_Gly109del
NM_000077.4:c.182_283del , LRG_11t1:c.182_283del	NP_000068.1:p.Glu61_Leu94del
NM_001195132.1:c.182_283del	NP_001182061.1:p.Glu61_Leu94del
NM_058195.3:c.225_326del , LRG_11t2:c.225_326del	NP_478102.2:p.Ala76_Gly109del
NM_058197.4:c.456_557del	NP_478104.2:n.456_557del
XM_005251343.1:c.29_130del	XP_005251400.1:p.Glu10_Leu43del
XM_011517675.1:c.182_283del	XP_011515977.1:p.Glu61_Leu94del
XM_011517676.1:c.182_283del	XP_011515978.1:p.Glu61_Leu94del
XM_011517679.1:c.29_130del	XP_011515981.1:p.Glu10_Leu43del
XR_929159.1:n.583_684del
XR_929161.1:n.372_473del
XR_929162.1:n.372_473del
XR_929163.1:n.321_422del
XR_929164.1:n.104_205del
NM_001363763.1:c.29_130del	NP_001350692.1:p.Glu10_Leu43del
XM_011517675.2:c.182_283del	XP_011515977.1:p.Glu61_Leu94del
XM_011517676.2:c.182_283del	XP_011515978.1:p.Glu61_Leu94del
XR_929159.2:n.512_613del
NM_001363763.2:c.29_130del	NP_001350692.1:p.Glu10_Leu43del
NM_000077.5:c.182_283del MANE Select	NP_000068.1:p.Glu61_Leu94del
NM_001195132.2:c.182_283del	NP_001182061.1:p.Glu61_Leu94del
NM_058195.4:c.225_326del MANE Plus Clinical	NP_478102.2:p.Ala76_Gly109del
NM_058197.5:c.*105_*206del	NP_478104.2:n.*105_*206del