Canonical Allele Identifier: CA1839161928

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971114_21971133delinsACGGGTCGGGTGAGAGTGGC , CM000671.2:g.21971114_21971133delinsACGGGTCGGGTGAGAGTGGC	GRCh38
NC_000009.11:g.21971113_21971132delinsACGGGTCGGGTGAGAGTGGC , CM000671.1:g.21971113_21971132delinsACGGGTCGGGTGAGAGTGGC	GRCh37
NC_000009.10:g.21961113_21961132delinsACGGGTCGGGTGAGAGTGGC	NCBI36
NG_007485.1:g.28359_28378delinsGCCACTCTCACCCGACCCGT , LRG_11:g.28359_28378delinsGCCACTCTCACCCGACCCGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.226_245delinsGCCACTCTCACCCGACCCGT MANE Select	ENSP00000307101.5:p.Ala76=
ENST00000404796.3:c.348-58319_348-58300delinsACGGGTCGGGTGAGAGTGGC	ENSP00000385916.2:n.348-58319_348-58300delinsACGGGTCGGGTGAGAG...
ENST00000579755.2:c.269_288delinsGCCACTCTCACCCGACCCGT MANE Plus Clinical	ENSP00000462950.1:p.Arg90=
ENST00000304494.9:c.226_245delinsGCCACTCTCACCCGACCCGT	ENSP00000307101.5:p.Ala76=
ENST00000361570.4:c.269_287delinsGCCACTCTCACCCGACCCGT
ENST00000380150.2:n.200_219delinsGCCACTCTCACCCGACCCGT
ENST00000380151.3:c.500_519delinsGCCACTCTCACCCGACCCGT	ENSP00000369496.3:n.500_519delinsGCCACTCTCACCCGACCCGT
ENST00000404796.2:c.348-58319_348-58300delinsACGGGTCGGGTGAGAGTGGC	ENSP00000385916.2:n.348-58319_348-58300delinsACGGGTCGGGTGAGAG...
ENST00000479692.2:c.73_92delinsGCCACTCTCACCCGACCCGT	ENSP00000466887.1:p.Ala25=
ENST00000494262.5:c.73_92delinsGCCACTCTCACCCGACCCGT	ENSP00000464952.1:p.Ala25=
ENST00000497750.1:c.73_92delinsGCCACTCTCACCCGACCCGT	ENSP00000468510.1:p.Ala25=
ENST00000498124.1:c.226_245delinsGCCACTCTCACCCGACCCGT	ENSP00000418915.1:p.Ala76=
ENST00000498628.6:c.73_92delinsGCCACTCTCACCCGACCCGT	ENSP00000467857.1:p.Ala25=
ENST00000530628.2:c.269_288delinsGCCACTCTCACCCGACCCGT	ENSP00000432664.2:p.Arg90=
ENST00000578845.2:c.73_92delinsGCCACTCTCACCCGACCCGT	ENSP00000467390.1:p.Ala25=
ENST00000579122.1:c.226_245delinsGCCACTCTCACCCGACCCGT	ENSP00000464202.1:p.Ala76=
ENST00000579755.1:c.269_288delinsGCCACTCTCACCCGACCCGT	ENSP00000462950.1:p.Arg90=
NM_000077.4:c.226_245delinsGCCACTCTCACCCGACCCGT , LRG_11t1:c.226_245delinsGCCACTCTCACCCGACCCGT	NP_000068.1:p.Ala76=
NM_001195132.1:c.226_245delinsGCCACTCTCACCCGACCCGT	NP_001182061.1:p.Ala76=
NM_058195.3:c.269_288delinsGCCACTCTCACCCGACCCGT , LRG_11t2:c.269_288delinsGCCACTCTCACCCGACCCGT	NP_478102.2:p.Arg90=
NM_058197.4:c.500_519delinsGCCACTCTCACCCGACCCGT	NP_478104.2:n.500_519delinsGCCACTCTCACCCGACCCGT
XM_005251343.1:c.73_92delinsGCCACTCTCACCCGACCCGT	XP_005251400.1:p.Ala25=
XM_011517675.1:c.226_245delinsGCCACTCTCACCCGACCCGT	XP_011515977.1:p.Ala76=
XM_011517676.1:c.226_245delinsGCCACTCTCACCCGACCCGT	XP_011515978.1:p.Ala76=
XM_011517679.1:c.73_92delinsGCCACTCTCACCCGACCCGT	XP_011515981.1:p.Ala25=
XR_929159.1:n.627_646delinsGCCACTCTCACCCGACCCGT
XR_929161.1:n.416_435delinsGCCACTCTCACCCGACCCGT
XR_929162.1:n.416_435delinsGCCACTCTCACCCGACCCGT
XR_929163.1:n.365_384delinsGCCACTCTCACCCGACCCGT
XR_929164.1:n.148_167delinsGCCACTCTCACCCGACCCGT
NM_001363763.1:c.73_92delinsGCCACTCTCACCCGACCCGT	NP_001350692.1:p.Ala25=
XM_011517675.2:c.226_245delinsGCCACTCTCACCCGACCCGT	XP_011515977.1:p.Ala76=
XM_011517676.2:c.226_245delinsGCCACTCTCACCCGACCCGT	XP_011515978.1:p.Ala76=
XR_929159.2:n.556_575delinsGCCACTCTCACCCGACCCGT
NM_001363763.2:c.73_92delinsGCCACTCTCACCCGACCCGT	NP_001350692.1:p.Ala25=
NM_000077.5:c.226_245delinsGCCACTCTCACCCGACCCGT MANE Select	NP_000068.1:p.Ala76=
NM_001195132.2:c.226_245delinsGCCACTCTCACCCGACCCGT	NP_001182061.1:p.Ala76=
NM_058195.4:c.269_288delinsGCCACTCTCACCCGACCCGT MANE Plus Clinical	NP_478102.2:p.Arg90=
NM_058197.5:c.*149_*168delinsGCCACTCTCACCCGACCCGT	NP_478104.2:n.*149_*168delinsGCCACTCTCACCCGACCCGT