Canonical Allele Identifier: CA1839162516

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971183A= , CM000671.2:g.21971183A=	GRCh38
NC_000009.11:g.21971182A= , CM000671.1:g.21971182A=	GRCh37
NC_000009.10:g.21961182A=	NCBI36
NG_007485.1:g.28309T= , LRG_11:g.28309T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.176T= MANE Select	ENSP00000307101.5:p.Val59=
ENST00000404796.3:c.348-58250A=	ENSP00000385916.2:n.348-58250A=
ENST00000579755.2:c.219T= MANE Plus Clinical	ENSP00000462950.1:p.Ser73=
ENST00000304494.9:c.176T=	ENSP00000307101.5:p.Val59=
ENST00000361570.4:c.219T=	ENSP00000355153.4:p.Ser73=
ENST00000380150.2:n.150T=
ENST00000380151.3:c.450T=	ENSP00000369496.3:n.450T=
ENST00000404796.2:c.348-58250A=	ENSP00000385916.2:n.348-58250A=
ENST00000479692.2:c.23T=	ENSP00000466887.1:p.Val8=
ENST00000494262.5:c.23T=	ENSP00000464952.1:p.Val8=
ENST00000497750.1:c.23T=	ENSP00000468510.1:p.Val8=
ENST00000498124.1:c.176T=	ENSP00000418915.1:p.Val59=
ENST00000498628.6:c.23T=	ENSP00000467857.1:p.Val8=
ENST00000530628.2:c.219T=	ENSP00000432664.2:p.Ser73=
ENST00000578845.2:c.23T=	ENSP00000467390.1:p.Val8=
ENST00000579122.1:c.176T=	ENSP00000464202.1:p.Val59=
ENST00000579755.1:c.219T=	ENSP00000462950.1:p.Ser73=
NM_000077.4:c.176T= , LRG_11t1:c.176T=	NP_000068.1:p.Val59=
NM_001195132.1:c.176T=	NP_001182061.1:p.Val59=
NM_058195.3:c.219T= , LRG_11t2:c.219T=	NP_478102.2:p.Ser73=
NM_058197.4:c.450T=	NP_478104.2:n.450T=
XM_005251343.1:c.23T=	XP_005251400.1:p.Val8=
XM_011517675.1:c.176T=	XP_011515977.1:p.Val59=
XM_011517676.1:c.176T=	XP_011515978.1:p.Val59=
XM_011517679.1:c.23T=	XP_011515981.1:p.Val8=
XR_929159.1:n.577T=
XR_929161.1:n.366T=
XR_929162.1:n.366T=
XR_929163.1:n.315T=
XR_929164.1:n.98T=
NM_001363763.1:c.23T=	NP_001350692.1:p.Val8=
XM_011517675.2:c.176T=	XP_011515977.1:p.Val59=
XM_011517676.2:c.176T=	XP_011515978.1:p.Val59=
XR_929159.2:n.506T=
NM_001363763.2:c.23T=	NP_001350692.1:p.Val8=
NM_000077.5:c.176T= MANE Select	NP_000068.1:p.Val59=
NM_001195132.2:c.176T=	NP_001182061.1:p.Val59=
NM_058195.4:c.219T= MANE Plus Clinical	NP_478102.2:p.Ser73=
NM_058197.5:c.*99T=	NP_478104.2:n.*99T=