Canonical Allele Identifier: CA1839160630

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21970909_21970910delinsAC , CM000671.2:g.21970909_21970910delinsAC	GRCh38
NC_000009.11:g.21970908_21970909delinsAC , CM000671.1:g.21970908_21970909delinsAC	GRCh37
NC_000009.10:g.21960908_21960909delinsAC	NCBI36
NG_007485.1:g.28582_28583delinsGT , LRG_11:g.28582_28583delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.449_450delinsGT MANE Select	ENSP00000307101.5:p.Gly150=
ENST00000404796.3:c.348-58524_348-58523delinsAC	ENSP00000385916.2:n.348-58524_348-58523delinsAC
ENST00000579755.2:c.*93_*94delinsGT MANE Plus Clinical	ENSP00000462950.1:n.*93_*94delinsGT
ENST00000304494.9:c.449_450delinsGT	ENSP00000307101.5:p.Gly150=
ENST00000361570.4:c.491_492delinsGT	ENSP00000355153.4:p.Gly164=
ENST00000380150.2:n.423_424delinsGT
ENST00000380151.3:c.723_724delinsGT	ENSP00000369496.3:n.723_724delinsGT
ENST00000404796.2:c.348-58524_348-58523delinsAC	ENSP00000385916.2:n.348-58524_348-58523delinsAC
ENST00000479692.2:c.296_297delinsGT	ENSP00000466887.1:p.Gly99=
ENST00000494262.5:c.296_297delinsGT	ENSP00000464952.1:p.Gly99=
ENST00000497750.1:c.296_297delinsGT	ENSP00000468510.1:p.Gly99=
ENST00000498124.1:c.449_450delinsGT	ENSP00000418915.1:p.Gly150=
ENST00000498628.6:c.296_297delinsGT	ENSP00000467857.1:p.Gly99=
ENST00000530628.2:c.*27+66_*27+67delinsGT	ENSP00000432664.2:n.*27+66_*27+67delinsGT
ENST00000578845.2:c.296_297delinsGT	ENSP00000467390.1:p.Gly99=
ENST00000579122.1:c.383+66_383+67delinsGT	ENSP00000464202.1:n.383+66_383+67delinsGT
ENST00000579755.1:c.*93_*94delinsGT	ENSP00000462950.1:n.*93_*94delinsGT
NM_000077.4:c.449_450delinsGT , LRG_11t1:c.449_450delinsGT	NP_000068.1:p.Gly150=
NM_001195132.1:c.449_450delinsGT	NP_001182061.1:p.Gly150=
NM_058195.3:c.*93_*94delinsGT , LRG_11t2:c.*93_*94delinsGT	NP_478102.2:n.*93_*94delinsGT
NM_058197.4:c.723_724delinsGT	NP_478104.2:n.723_724delinsGT
XM_005251343.1:c.296_297delinsGT	XP_005251400.1:p.Gly99=
XM_011517675.1:c.449_450delinsGT	XP_011515977.1:p.Gly150=
XM_011517676.1:c.449_450delinsGT	XP_011515978.1:p.Gly150=
XM_011517679.1:c.296_297delinsGT	XP_011515981.1:p.Gly99=
XR_929159.1:n.850_851delinsGT
XR_929161.1:n.639_640delinsGT
XR_929162.1:n.639_640delinsGT
XR_929163.1:n.588_589delinsGT
XR_929164.1:n.371_372delinsGT
NM_001363763.1:c.296_297delinsGT	NP_001350692.1:p.Gly99=
XM_011517675.2:c.449_450delinsGT	XP_011515977.1:p.Gly150=
XM_011517676.2:c.449_450delinsGT	XP_011515978.1:p.Gly150=
XR_929159.2:n.779_780delinsGT
NM_001363763.2:c.296_297delinsGT	NP_001350692.1:p.Gly99=
NM_000077.5:c.449_450delinsGT MANE Select	NP_000068.1:p.Gly150=
NM_001195132.2:c.449_450delinsGT	NP_001182061.1:p.Gly150=
NM_058195.4:c.*93_*94delinsGT MANE Plus Clinical	NP_478102.2:n.*93_*94delinsGT
NM_058197.5:c.*372_*373delinsGT	NP_478104.2:n.*372_*373delinsGT