Canonical Allele Identifier: CA1839173447

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974797_21974798delinsGC , CM000671.2:g.21974797_21974798delinsGC	GRCh38
NC_000009.11:g.21974796_21974797delinsGC , CM000671.1:g.21974796_21974797delinsGC	GRCh37
NC_000009.10:g.21964796_21964797delinsGC	NCBI36
NG_007485.1:g.24694_24695delinsGC , LRG_11:g.24694_24695delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.30_31delinsGC MANE Select	ENSP00000307101.5:p.Glu10=
ENST00000404796.3:c.348-54636_348-54635delinsGC	ENSP00000385916.2:n.348-54636_348-54635delinsGC
ENST00000579755.2:c.194-3590_194-3589delinsGC MANE Plus Clinical	ENSP00000462950.1:n.194-3590_194-3589delinsGC
ENST00000304494.9:c.30_31delinsGC	ENSP00000307101.5:p.Glu10=
ENST00000361570.4:c.194-3590_194-3589delinsGC	ENSP00000355153.4:n.194-3590_194-3589delinsGC
ENST00000380151.3:c.30_31delinsGC	ENSP00000369496.3:p.Glu10=
ENST00000404796.2:c.348-54636_348-54635delinsGC	ENSP00000385916.2:n.348-54636_348-54635delinsGC
ENST00000494262.5:c.-3-3590_-3-3589delinsGC	ENSP00000464952.1:n.-3-3590_-3-3589delinsGC
ENST00000498124.1:c.30_31delinsGC	ENSP00000418915.1:p.Glu10=
ENST00000498628.6:c.-3-3590_-3-3589delinsGC	ENSP00000467857.1:n.-3-3590_-3-3589delinsGC
ENST00000530628.2:c.194-3590_194-3589delinsGC	ENSP00000432664.2:n.194-3590_194-3589delinsGC
ENST00000579122.1:c.30_31delinsGC	ENSP00000464202.1:p.Glu10=
ENST00000579755.1:c.194-3590_194-3589delinsGC	ENSP00000462950.1:n.194-3590_194-3589delinsGC
NM_000077.4:c.30_31delinsGC , LRG_11t1:c.30_31delinsGC	NP_000068.1:p.Glu10=
NM_001195132.1:c.30_31delinsGC	NP_001182061.1:p.Glu10=
NM_058195.3:c.194-3590_194-3589delinsGC , LRG_11t2:c.194-3590_194-3589delinsGC	NP_478102.2:n.194-3590_194-3589delinsGC
NM_058197.4:c.30_31delinsGC	NP_478104.2:p.Glu10=
XM_011517675.1:c.30_31delinsGC	XP_011515977.1:p.Glu10=
XM_011517676.1:c.30_31delinsGC	XP_011515978.1:p.Glu10=
XM_011517679.1:c.-3-3590_-3-3589delinsGC	XP_011515981.1:n.-3-3590_-3-3589delinsGC
XR_929159.1:n.431_432delinsGC
XR_929161.1:n.341-3590_341-3589delinsGC
XR_929162.1:n.341-3590_341-3589delinsGC
XR_929163.1:n.290-3590_290-3589delinsGC
NM_001363763.1:c.-3-3590_-3-3589delinsGC	NP_001350692.1:n.-3-3590_-3-3589delinsGC
XM_011517675.2:c.30_31delinsGC	XP_011515977.1:p.Glu10=
XM_011517676.2:c.30_31delinsGC	XP_011515978.1:p.Glu10=
XR_929159.2:n.360_361delinsGC
NM_001363763.2:c.-3-3590_-3-3589delinsGC	NP_001350692.1:n.-3-3590_-3-3589delinsGC
NM_000077.5:c.30_31delinsGC MANE Select	NP_000068.1:p.Glu10=
NM_001195132.2:c.30_31delinsGC	NP_001182061.1:p.Glu10=
NM_058195.4:c.194-3590_194-3589delinsGC MANE Plus Clinical	NP_478102.2:n.194-3590_194-3589delinsGC
NM_058197.5:c.30_31delinsGC	NP_478104.2:p.Glu10=