Canonical Allele Identifier: CA1839160747

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21970951_21970952delinsGC , CM000671.2:g.21970951_21970952delinsGC	GRCh38
NC_000009.11:g.21970950_21970951delinsGC , CM000671.1:g.21970950_21970951delinsGC	GRCh37
NC_000009.10:g.21960950_21960951delinsGC	NCBI36
NG_007485.1:g.28540_28541delinsGC , LRG_11:g.28540_28541delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.407_408delinsGC MANE Select	ENSP00000307101.5:p.Gly136=
ENST00000404796.3:c.348-58482_348-58481delinsGC	ENSP00000385916.2:n.348-58482_348-58481delinsGC
ENST00000579755.2:c.*51_*52delinsGC MANE Plus Clinical	ENSP00000462950.1:n.*51_*52delinsGC
ENST00000304494.9:c.407_408delinsGC	ENSP00000307101.5:p.Gly136=
ENST00000361570.4:c.449_450delinsGC	ENSP00000355153.4:p.Gly150=
ENST00000380150.2:n.381_382delinsGC
ENST00000380151.3:c.681_682delinsGC	ENSP00000369496.3:n.681_682delinsGC
ENST00000404796.2:c.348-58482_348-58481delinsGC	ENSP00000385916.2:n.348-58482_348-58481delinsGC
ENST00000479692.2:c.254_255delinsGC	ENSP00000466887.1:p.Gly85=
ENST00000494262.5:c.254_255delinsGC	ENSP00000464952.1:p.Gly85=
ENST00000497750.1:c.254_255delinsGC	ENSP00000468510.1:p.Gly85=
ENST00000498124.1:c.407_408delinsGC	ENSP00000418915.1:p.Gly136=
ENST00000498628.6:c.254_255delinsGC	ENSP00000467857.1:p.Gly85=
ENST00000530628.2:c.*27+24_*27+25delinsGC	ENSP00000432664.2:n.*27+24_*27+25delinsGC
ENST00000578845.2:c.254_255delinsGC	ENSP00000467390.1:p.Gly85=
ENST00000579122.1:c.383+24_383+25delinsGC	ENSP00000464202.1:n.383+24_383+25delinsGC
ENST00000579755.1:c.*51_*52delinsGC	ENSP00000462950.1:n.*51_*52delinsGC
NM_000077.4:c.407_408delinsGC , LRG_11t1:c.407_408delinsGC	NP_000068.1:p.Gly136=
NM_001195132.1:c.407_408delinsGC	NP_001182061.1:p.Gly136=
NM_058195.3:c.*51_*52delinsGC , LRG_11t2:c.*51_*52delinsGC	NP_478102.2:n.*51_*52delinsGC
NM_058197.4:c.681_682delinsGC	NP_478104.2:n.681_682delinsGC
XM_005251343.1:c.254_255delinsGC	XP_005251400.1:p.Gly85=
XM_011517675.1:c.407_408delinsGC	XP_011515977.1:p.Gly136=
XM_011517676.1:c.407_408delinsGC	XP_011515978.1:p.Gly136=
XM_011517679.1:c.254_255delinsGC	XP_011515981.1:p.Gly85=
XR_929159.1:n.808_809delinsGC
XR_929161.1:n.597_598delinsGC
XR_929162.1:n.597_598delinsGC
XR_929163.1:n.546_547delinsGC
XR_929164.1:n.329_330delinsGC
NM_001363763.1:c.254_255delinsGC	NP_001350692.1:p.Gly85=
XM_011517675.2:c.407_408delinsGC	XP_011515977.1:p.Gly136=
XM_011517676.2:c.407_408delinsGC	XP_011515978.1:p.Gly136=
XR_929159.2:n.737_738delinsGC
NM_001363763.2:c.254_255delinsGC	NP_001350692.1:p.Gly85=
NM_000077.5:c.407_408delinsGC MANE Select	NP_000068.1:p.Gly136=
NM_001195132.2:c.407_408delinsGC	NP_001182061.1:p.Gly136=
NM_058195.4:c.*51_*52delinsGC MANE Plus Clinical	NP_478102.2:n.*51_*52delinsGC
NM_058197.5:c.*330_*331delinsGC	NP_478104.2:n.*330_*331delinsGC