Canonical Allele Identifier: CA1839173317

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974773_21974778delinsCCGTGG , CM000671.2:g.21974773_21974778delinsCCGTGG	GRCh38
NC_000009.11:g.21974772_21974777delinsCCGTGG , CM000671.1:g.21974772_21974777delinsCCGTGG	GRCh37
NC_000009.10:g.21964772_21964777delinsCCGTGG	NCBI36
NG_007485.1:g.24714_24719delinsCCACGG , LRG_11:g.24714_24719delinsCCACGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.50_55delinsCCACGG MANE Select	ENSP00000307101.5:p.Ala17=
ENST00000404796.3:c.348-54660_348-54655delinsCCGTGG	ENSP00000385916.2:n.348-54660_348-54655delinsCCGTGG
ENST00000579755.2:c.194-3570_194-3565delinsCCACGG MANE Plus Clinical	ENSP00000462950.1:n.194-3570_194-3565delinsCCACGG
ENST00000304494.9:c.50_55delinsCCACGG	ENSP00000307101.5:p.Ala17=
ENST00000361570.4:c.194-3570_194-3565delinsCCACGG	ENSP00000355153.4:n.194-3570_194-3565delinsCCACGG
ENST00000380151.3:c.50_55delinsCCACGG	ENSP00000369496.3:p.Ala17=
ENST00000404796.2:c.348-54660_348-54655delinsCCGTGG	ENSP00000385916.2:n.348-54660_348-54655delinsCCGTGG
ENST00000494262.5:c.-3-3570_-3-3565delinsCCACGG	ENSP00000464952.1:n.-3-3570_-3-3565delinsCCACGG
ENST00000498124.1:c.50_55delinsCCACGG	ENSP00000418915.1:p.Ala17=
ENST00000498628.6:c.-3-3570_-3-3565delinsCCACGG	ENSP00000467857.1:n.-3-3570_-3-3565delinsCCACGG
ENST00000530628.2:c.194-3570_194-3565delinsCCACGG	ENSP00000432664.2:n.194-3570_194-3565delinsCCACGG
ENST00000579122.1:c.50_55delinsCCACGG	ENSP00000464202.1:p.Ala17=
ENST00000579755.1:c.194-3570_194-3565delinsCCACGG	ENSP00000462950.1:n.194-3570_194-3565delinsCCACGG
NM_000077.4:c.50_55delinsCCACGG , LRG_11t1:c.50_55delinsCCACGG	NP_000068.1:p.Ala17=
NM_001195132.1:c.50_55delinsCCACGG	NP_001182061.1:p.Ala17=
NM_058195.3:c.194-3570_194-3565delinsCCACGG , LRG_11t2:c.194-3570_194-3565delinsCCACGG	NP_478102.2:n.194-3570_194-3565delinsCCACGG
NM_058197.4:c.50_55delinsCCACGG	NP_478104.2:p.Ala17=
XM_011517675.1:c.50_55delinsCCACGG	XP_011515977.1:p.Ala17=
XM_011517676.1:c.50_55delinsCCACGG	XP_011515978.1:p.Ala17=
XM_011517679.1:c.-3-3570_-3-3565delinsCCACGG	XP_011515981.1:n.-3-3570_-3-3565delinsCCACGG
XR_929159.1:n.451_456delinsCCACGG
XR_929161.1:n.341-3570_341-3565delinsCCACGG
XR_929162.1:n.341-3570_341-3565delinsCCACGG
XR_929163.1:n.290-3570_290-3565delinsCCACGG
NM_001363763.1:c.-3-3570_-3-3565delinsCCACGG	NP_001350692.1:n.-3-3570_-3-3565delinsCCACGG
XM_011517675.2:c.50_55delinsCCACGG	XP_011515977.1:p.Ala17=
XM_011517676.2:c.50_55delinsCCACGG	XP_011515978.1:p.Ala17=
XR_929159.2:n.380_385delinsCCACGG
NM_001363763.2:c.-3-3570_-3-3565delinsCCACGG	NP_001350692.1:n.-3-3570_-3-3565delinsCCACGG
NM_000077.5:c.50_55delinsCCACGG MANE Select	NP_000068.1:p.Ala17=
NM_001195132.2:c.50_55delinsCCACGG	NP_001182061.1:p.Ala17=
NM_058195.4:c.194-3570_194-3565delinsCCACGG MANE Plus Clinical	NP_478102.2:n.194-3570_194-3565delinsCCACGG
NM_058197.5:c.50_55delinsCCACGG	NP_478104.2:p.Ala17=