Canonical Allele Identifier: CA1839173430

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974795_21974819delinsAGGCTCCATGCTGCTCCCCGCCGCC , CM000671.2:g.21974795_21974819delinsAGGCTCCATGCTGCTCCCCGCCGCC	GRCh38
NC_000009.11:g.21974794_21974818delinsAGGCTCCATGCTGCTCCCCGCCGCC , CM000671.1:g.21974794_21974818delinsAGGCTCCATGCTGCTCCCCGCCGCC	GRCh37
NC_000009.10:g.21964794_21964818delinsAGGCTCCATGCTGCTCCCCGCCGCC	NCBI36
NG_007485.1:g.24673_24697delinsGGCGGCGGGGAGCAGCATGGAGCCT , LRG_11:g.24673_24697delinsGGCGGCGGGGAGCAGCATGGAGCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT MANE Select	ENSP00000307101.5:p.Pro3=
ENST00000404796.3:c.348-54638_348-54614delinsAGGCTCCATGCTGCTCCCCGCCGCC	ENSP00000385916.2:n.348-54638_348-54614delinsAGGCTCCATGCTGCTC...
ENST00000579755.2:c.194-3611_194-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT MANE Plus Clinical	ENSP00000462950.1:n.194-3611_194-3587delinsGGCGGCGGGGAGCAGCAT...
ENST00000304494.9:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT	ENSP00000307101.5:p.Pro3=
ENST00000361570.4:c.194-3611_194-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT	ENSP00000355153.4:n.194-3611_194-3587delinsGGCGGCGGGGAGCAGCAT...
ENST00000380151.3:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT	ENSP00000369496.3:p.Pro3=
ENST00000404796.2:c.348-54638_348-54614delinsAGGCTCCATGCTGCTCCCCGCCGCC	ENSP00000385916.2:n.348-54638_348-54614delinsAGGCTCCATGCTGCTC...
ENST00000494262.5:c.-3-3611_-3-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT	ENSP00000464952.1:n.-3-3611_-3-3587delinsGGCGGCGGGGAGCAGCATGG...
ENST00000498124.1:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT	ENSP00000418915.1:p.Pro3=
ENST00000498628.6:c.-3-3611_-3-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT	ENSP00000467857.1:n.-3-3611_-3-3587delinsGGCGGCGGGGAGCAGCATGG...
ENST00000530628.2:c.194-3611_194-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT	ENSP00000432664.2:n.194-3611_194-3587delinsGGCGGCGGGGAGCAGCAT...
ENST00000579122.1:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT	ENSP00000464202.1:p.Pro3=
ENST00000579755.1:c.194-3611_194-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT	ENSP00000462950.1:n.194-3611_194-3587delinsGGCGGCGGGGAGCAGCAT...
NM_000077.4:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT , LRG_11t1:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT	NP_000068.1:p.Pro3=
NM_001195132.1:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT	NP_001182061.1:p.Pro3=
NM_058195.3:c.194-3611_194-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT , LRG_11t2:c.194-3611_194-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT	NP_478102.2:n.194-3611_194-3587delinsGGCGGCGGGGAGCAGCATGGAGCC...
NM_058197.4:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT	NP_478104.2:p.Pro3=
XM_011517675.1:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT	XP_011515977.1:p.Pro3=
XM_011517676.1:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT	XP_011515978.1:p.Pro3=
XM_011517679.1:c.-3-3611_-3-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT	XP_011515981.1:n.-3-3611_-3-3587delinsGGCGGCGGGGAGCAGCATGGAGC...
XR_929159.1:n.410_434delinsGGCGGCGGGGAGCAGCATGGAGCCT
XR_929161.1:n.341-3611_341-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT
XR_929162.1:n.341-3611_341-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT
XR_929163.1:n.290-3611_290-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT
NM_001363763.1:c.-3-3611_-3-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT	NP_001350692.1:n.-3-3611_-3-3587delinsGGCGGCGGGGAGCAGCATGGAGC...
XM_011517675.2:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT	XP_011515977.1:p.Pro3=
XM_011517676.2:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT	XP_011515978.1:p.Pro3=
XR_929159.2:n.339_363delinsGGCGGCGGGGAGCAGCATGGAGCCT
NM_001363763.2:c.-3-3611_-3-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT	NP_001350692.1:n.-3-3611_-3-3587delinsGGCGGCGGGGAGCAGCATGGAGC...
NM_000077.5:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT MANE Select	NP_000068.1:p.Pro3=
NM_001195132.2:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT	NP_001182061.1:p.Pro3=
NM_058195.4:c.194-3611_194-3587delinsGGCGGCGGGGAGCAGCATGGAGCCT MANE Plus Clinical	NP_478102.2:n.194-3611_194-3587delinsGGCGGCGGGGAGCAGCATGGAGCC...
NM_058197.5:c.9_33delinsGGCGGCGGGGAGCAGCATGGAGCCT	NP_478104.2:p.Pro3=