Canonical Allele Identifier: CA645552607

Gene: CDKN2A

Linked Data

• COSMIC: COSM4949755 ; COSM4949756 ; COSM4949757

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974713_21974730del , CM000671.2:g.21974713_21974730del	GRCh38
NC_000009.11:g.21974712_21974729del , CM000671.1:g.21974712_21974729del	GRCh37
NC_000009.10:g.21964712_21964729del	NCBI36
NG_007485.1:g.24763_24780del , LRG_11:g.24763_24780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.99_116del MANE Select	ENSP00000307101.5:p.Glu33_Asn39delinsAsp
ENST00000404796.3:c.348-54720_348-54703del	ENSP00000385916.2:n.348-54720_348-54703del
ENST00000579755.2:c.194-3521_194-3504del MANE Plus Clinical	ENSP00000462950.1:n.194-3521_194-3504del
ENST00000304494.9:c.99_116del	ENSP00000307101.5:p.Glu33_Asn39delinsAsp
ENST00000361570.4:c.194-3521_194-3504del	ENSP00000355153.4:n.194-3521_194-3504del
ENST00000380151.3:c.99_116del	ENSP00000369496.3:p.Glu33_Asn39delinsAsp
ENST00000404796.2:c.348-54720_348-54703del	ENSP00000385916.2:n.348-54720_348-54703del
ENST00000494262.5:c.-3-3521_-3-3504del	ENSP00000464952.1:n.-3-3521_-3-3504del
ENST00000498124.1:c.99_116del	ENSP00000418915.1:p.Glu33_Asn39delinsAsp
ENST00000498628.6:c.-3-3521_-3-3504del	ENSP00000467857.1:n.-3-3521_-3-3504del
ENST00000530628.2:c.194-3521_194-3504del	ENSP00000432664.2:n.194-3521_194-3504del
ENST00000579122.1:c.99_116del	ENSP00000464202.1:p.Glu33_Asn39delinsAsp
ENST00000579755.1:c.194-3521_194-3504del	ENSP00000462950.1:n.194-3521_194-3504del
NM_000077.4:c.99_116del , LRG_11t1:c.99_116del	NP_000068.1:p.Glu33_Asn39delinsAsp
NM_001195132.1:c.99_116del	NP_001182061.1:p.Glu33_Asn39delinsAsp
NM_058195.3:c.194-3521_194-3504del , LRG_11t2:c.194-3521_194-3504del	NP_478102.2:n.194-3521_194-3504del
NM_058197.4:c.99_116del	NP_478104.2:p.Glu33_Asn39delinsAsp
XM_011517675.1:c.99_116del	XP_011515977.1:p.Glu33_Asn39delinsAsp
XM_011517676.1:c.99_116del	XP_011515978.1:p.Glu33_Asn39delinsAsp
XM_011517679.1:c.-3-3521_-3-3504del	XP_011515981.1:n.-3-3521_-3-3504del
XR_929159.1:n.500_517del
XR_929161.1:n.341-3521_341-3504del
XR_929162.1:n.341-3521_341-3504del
XR_929163.1:n.290-3521_290-3504del
NM_001363763.1:c.-3-3521_-3-3504del	NP_001350692.1:n.-3-3521_-3-3504del
XM_011517675.2:c.99_116del	XP_011515977.1:p.Glu33_Asn39delinsAsp
XM_011517676.2:c.99_116del	XP_011515978.1:p.Glu33_Asn39delinsAsp
XR_929159.2:n.429_446del
NM_001363763.2:c.-3-3521_-3-3504del	NP_001350692.1:n.-3-3521_-3-3504del
NM_000077.5:c.99_116del MANE Select	NP_000068.1:p.Glu33_Asn39delinsAsp
NM_001195132.2:c.99_116del	NP_001182061.1:p.Glu33_Asn39delinsAsp
NM_058195.4:c.194-3521_194-3504del MANE Plus Clinical	NP_478102.2:n.194-3521_194-3504del
NM_058197.5:c.99_116del	NP_478104.2:p.Glu33_Asn39delinsAsp