Canonical Allele Identifier: CA1839172723

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974679T= , CM000671.2:g.21974679T=	GRCh38
NC_000009.11:g.21974678T= , CM000671.1:g.21974678T=	GRCh37
NC_000009.10:g.21964678T=	NCBI36
NG_007485.1:g.24813A= , LRG_11:g.24813A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.149A= MANE Select	ENSP00000307101.5:p.Gln50=
ENST00000404796.3:c.348-54754T=	ENSP00000385916.2:n.348-54754T=
ENST00000579755.2:c.194-3471A= MANE Plus Clinical	ENSP00000462950.1:n.194-3471A=
ENST00000304494.9:c.149A=	ENSP00000307101.5:p.Gln50=
ENST00000361570.4:c.194-3471A=	ENSP00000355153.4:n.194-3471A=
ENST00000380151.3:c.149A=	ENSP00000369496.3:p.Gln50=
ENST00000404796.2:c.348-54754T=	ENSP00000385916.2:n.348-54754T=
ENST00000494262.5:c.-3-3471A=	ENSP00000464952.1:n.-3-3471A=
ENST00000498124.1:c.149A=	ENSP00000418915.1:p.Gln50=
ENST00000498628.6:c.-3-3471A=	ENSP00000467857.1:n.-3-3471A=
ENST00000530628.2:c.194-3471A=	ENSP00000432664.2:n.194-3471A=
ENST00000579122.1:c.149A=	ENSP00000464202.1:p.Gln50=
ENST00000579755.1:c.194-3471A=	ENSP00000462950.1:n.194-3471A=
NM_000077.4:c.149A= , LRG_11t1:c.149A=	NP_000068.1:p.Gln50=
NM_001195132.1:c.149A=	NP_001182061.1:p.Gln50=
NM_058195.3:c.194-3471A= , LRG_11t2:c.194-3471A=	NP_478102.2:n.194-3471A=
NM_058197.4:c.149A=	NP_478104.2:p.Gln50=
XM_011517675.1:c.149A=	XP_011515977.1:p.Gln50=
XM_011517676.1:c.149A=	XP_011515978.1:p.Gln50=
XM_011517679.1:c.-3-3471A=	XP_011515981.1:n.-3-3471A=
XR_929159.1:n.550A=
XR_929161.1:n.341-3471A=
XR_929162.1:n.341-3471A=
XR_929163.1:n.290-3471A=
NM_001363763.1:c.-3-3471A=	NP_001350692.1:n.-3-3471A=
XM_011517675.2:c.149A=	XP_011515977.1:p.Gln50=
XM_011517676.2:c.149A=	XP_011515978.1:p.Gln50=
XR_929159.2:n.479A=
NM_001363763.2:c.-3-3471A=	NP_001350692.1:n.-3-3471A=
NM_000077.5:c.149A= MANE Select	NP_000068.1:p.Gln50=
NM_001195132.2:c.149A=	NP_001182061.1:p.Gln50=
NM_058195.4:c.194-3471A= MANE Plus Clinical	NP_478102.2:n.194-3471A=
NM_058197.5:c.149A=	NP_478104.2:p.Gln50=