Canonical Allele Identifier: CA464261890

Gene: CDKN2A

Linked Data

• MyVariant Identifiers: chr9:g.21971204_21971205insT (hg19) ; chr9:g.21971203_21971204insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971205dup , CM000671.2:g.21971205dup	GRCh38
NC_000009.11:g.21971204dup , CM000671.1:g.21971204dup	GRCh37
NC_000009.10:g.21961204dup	NCBI36
NG_007485.1:g.28287dup , LRG_11:g.28287dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.154dup MANE Select	ENSP00000307101.5:p.Met52AsnfsTer?
ENST00000404796.3:c.348-58228dup	ENSP00000385916.2:n.348-58228dup
ENST00000579755.2:c.197dup MANE Plus Clinical	ENSP00000462950.1:p.His66GlnfsTer2
ENST00000304494.9:c.154dup	ENSP00000307101.5:p.Met52AsnfsTer?
ENST00000361570.4:c.197dup	ENSP00000355153.4:p.His66GlnfsTer2
ENST00000380150.2:n.128dup
ENST00000380151.3:c.428dup	ENSP00000369496.3:n.428dup
ENST00000404796.2:c.348-58228dup	ENSP00000385916.2:n.348-58228dup
ENST00000479692.2:c.1dup	ENSP00000466887.1:p.Met1AsnfsTer?
ENST00000494262.5:c.1dup	ENSP00000464952.1:p.Met1AsnfsTer?
ENST00000497750.1:c.1dup	ENSP00000468510.1:p.Met1AsnfsTer?
ENST00000498124.1:c.154dup	ENSP00000418915.1:p.Met52AsnfsTer?
ENST00000498628.6:c.1dup	ENSP00000467857.1:p.Met1AsnfsTer?
ENST00000530628.2:c.197dup	ENSP00000432664.2:p.His66GlnfsTer2
ENST00000578845.2:c.1dup	ENSP00000467390.1:p.Met1AsnfsTer?
ENST00000579122.1:c.154dup	ENSP00000464202.1:p.Met52AsnfsTer?
ENST00000579755.1:c.197dup	ENSP00000462950.1:p.His66GlnfsTer2
NM_000077.4:c.154dup , LRG_11t1:c.154dup	NP_000068.1:p.Met52AsnfsTer?
NM_001195132.1:c.154dup	NP_001182061.1:p.Met52AsnfsTer?
NM_058195.3:c.197dup , LRG_11t2:c.197dup	NP_478102.2:p.His66GlnfsTer2
NM_058197.4:c.428dup	NP_478104.2:n.428dup
XM_005251343.1:c.1dup	XP_005251400.1:p.Met1AsnfsTer?
XM_011517675.1:c.154dup	XP_011515977.1:p.Met52AsnfsTer?
XM_011517676.1:c.154dup	XP_011515978.1:p.Met52AsnfsTer?
XM_011517679.1:c.1dup	XP_011515981.1:p.Met1AsnfsTer?
XR_929159.1:n.555dup
XR_929161.1:n.344dup
XR_929162.1:n.344dup
XR_929163.1:n.293dup
XR_929164.1:n.76dup
NM_001363763.1:c.1dup	NP_001350692.1:p.Met1AsnfsTer?
XM_011517675.2:c.154dup	XP_011515977.1:p.Met52AsnfsTer?
XM_011517676.2:c.154dup	XP_011515978.1:p.Met52AsnfsTer?
XR_929159.2:n.484dup
NM_001363763.2:c.1dup	NP_001350692.1:p.Met1AsnfsTer?
NM_000077.5:c.154dup MANE Select	NP_000068.1:p.Met52AsnfsTer?
NM_001195132.2:c.154dup	NP_001182061.1:p.Met52AsnfsTer?
NM_058195.4:c.197dup MANE Plus Clinical	NP_478102.2:p.His66GlnfsTer2
NM_058197.5:c.*77dup	NP_478104.2:n.*77dup