Canonical Allele Identifier: CA1839161948

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971115_21971134delinsCGGGTCGGGTGAGAGTGGCG , CM000671.2:g.21971115_21971134delinsCGGGTCGGGTGAGAGTGGCG	GRCh38
NC_000009.11:g.21971114_21971133delinsCGGGTCGGGTGAGAGTGGCG , CM000671.1:g.21971114_21971133delinsCGGGTCGGGTGAGAGTGGCG	GRCh37
NC_000009.10:g.21961114_21961133delinsCGGGTCGGGTGAGAGTGGCG	NCBI36
NG_007485.1:g.28358_28377delinsCGCCACTCTCACCCGACCCG , LRG_11:g.28358_28377delinsCGCCACTCTCACCCGACCCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.225_244delinsCGCCACTCTCACCCGACCCG MANE Select	ENSP00000307101.5:p.Pro75=
ENST00000404796.3:c.348-58318_348-58299delinsCGGGTCGGGTGAGAGTGGCG	ENSP00000385916.2:n.348-58318_348-58299de...
ENST00000579755.2:c.268_287delinsCGCCACTCTCACCCGACCCG MANE Plus Clinical	ENSP00000462950.1:p.Arg90=
ENST00000304494.9:c.225_244delinsCGCCACTCTCACCCGACCCG	ENSP00000307101.5:p.Pro75=
ENST00000361570.4:c.268_286delinsCGCCACTCTCACCCGACCCG
ENST00000380150.2:n.199_218delinsCGCCACTCTCACCCGACCCG
ENST00000380151.3:c.499_518delinsCGCCACTCTCACCCGACCCG	ENSP00000369496.3:n.499_518delinsCGCCACTC...
ENST00000404796.2:c.348-58318_348-58299delinsCGGGTCGGGTGAGAGTGGCG	ENSP00000385916.2:n.348-58318_348-58299de...
ENST00000479692.2:c.72_91delinsCGCCACTCTCACCCGACCCG	ENSP00000466887.1:p.Pro24=
ENST00000494262.5:c.72_91delinsCGCCACTCTCACCCGACCCG	ENSP00000464952.1:p.Pro24=
ENST00000497750.1:c.72_91delinsCGCCACTCTCACCCGACCCG	ENSP00000468510.1:p.Pro24=
ENST00000498124.1:c.225_244delinsCGCCACTCTCACCCGACCCG	ENSP00000418915.1:p.Pro75=
ENST00000498628.6:c.72_91delinsCGCCACTCTCACCCGACCCG	ENSP00000467857.1:p.Pro24=
ENST00000530628.2:c.268_287delinsCGCCACTCTCACCCGACCCG	ENSP00000432664.2:p.Arg90=
ENST00000578845.2:c.72_91delinsCGCCACTCTCACCCGACCCG	ENSP00000467390.1:p.Pro24=
ENST00000579122.1:c.225_244delinsCGCCACTCTCACCCGACCCG	ENSP00000464202.1:p.Pro75=
ENST00000579755.1:c.268_287delinsCGCCACTCTCACCCGACCCG	ENSP00000462950.1:p.Arg90=
NM_000077.4:c.225_244delinsCGCCACTCTCACCCGACCCG , LRG_11t1:c.225_244delinsCGCCACTCTCACCCGACCCG	NP_000068.1:p.Pro75=
NM_001195132.1:c.225_244delinsCGCCACTCTCACCCGACCCG	NP_001182061.1:p.Pro75=
NM_058195.3:c.268_287delinsCGCCACTCTCACCCGACCCG , LRG_11t2:c.268_287delinsCGCCACTCTCACCCGACCCG	NP_478102.2:p.Arg90=
NM_058197.4:c.499_518delinsCGCCACTCTCACCCGACCCG	NP_478104.2:n.499_518delinsCGCCACTCTCACCC...
XM_005251343.1:c.72_91delinsCGCCACTCTCACCCGACCCG	XP_005251400.1:p.Pro24=
XM_011517675.1:c.225_244delinsCGCCACTCTCACCCGACCCG	XP_011515977.1:p.Pro75=
XM_011517676.1:c.225_244delinsCGCCACTCTCACCCGACCCG	XP_011515978.1:p.Pro75=
XM_011517679.1:c.72_91delinsCGCCACTCTCACCCGACCCG	XP_011515981.1:p.Pro24=
XR_929159.1:n.626_645delinsCGCCACTCTCACCCGACCCG
XR_929161.1:n.415_434delinsCGCCACTCTCACCCGACCCG
XR_929162.1:n.415_434delinsCGCCACTCTCACCCGACCCG
XR_929163.1:n.364_383delinsCGCCACTCTCACCCGACCCG
XR_929164.1:n.147_166delinsCGCCACTCTCACCCGACCCG
NM_001363763.1:c.72_91delinsCGCCACTCTCACCCGACCCG	NP_001350692.1:p.Pro24=
XM_011517675.2:c.225_244delinsCGCCACTCTCACCCGACCCG	XP_011515977.1:p.Pro75=
XM_011517676.2:c.225_244delinsCGCCACTCTCACCCGACCCG	XP_011515978.1:p.Pro75=
XR_929159.2:n.555_574delinsCGCCACTCTCACCCGACCCG
NM_001363763.2:c.72_91delinsCGCCACTCTCACCCGACCCG	NP_001350692.1:p.Pro24=
NM_000077.5:c.225_244delinsCGCCACTCTCACCCGACCCG MANE Select	NP_000068.1:p.Pro75=
NM_001195132.2:c.225_244delinsCGCCACTCTCACCCGACCCG	NP_001182061.1:p.Pro75=
NM_058195.4:c.268_287delinsCGCCACTCTCACCCGACCCG MANE Plus Clinical	NP_478102.2:p.Arg90=
NM_058197.5:c.*148_*167delinsCGCCACTCTCACCCGACCCG	NP_478104.2:n.*148_*167delinsCGCCACTCTCAC...