Canonical Allele Identifier: CA1839160706

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21970933A= , CM000671.2:g.21970933A=	GRCh38
NC_000009.11:g.21970932A= , CM000671.1:g.21970932A=	GRCh37
NC_000009.10:g.21960932A=	NCBI36
NG_007485.1:g.28559T= , LRG_11:g.28559T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.426T= MANE Select	ENSP00000307101.5:p.His142=
ENST00000404796.3:c.348-58500A=	ENSP00000385916.2:n.348-58500A=
ENST00000579755.2:c.*70T= MANE Plus Clinical	ENSP00000462950.1:n.*70T=
ENST00000304494.9:c.426T=	ENSP00000307101.5:p.His142=
ENST00000361570.4:c.468T=	ENSP00000355153.4:p.His156=
ENST00000380150.2:n.400T=
ENST00000380151.3:c.700T=	ENSP00000369496.3:n.700T=
ENST00000404796.2:c.348-58500A=	ENSP00000385916.2:n.348-58500A=
ENST00000479692.2:c.273T=	ENSP00000466887.1:p.His91=
ENST00000494262.5:c.273T=	ENSP00000464952.1:p.His91=
ENST00000497750.1:c.273T=	ENSP00000468510.1:p.His91=
ENST00000498124.1:c.426T=	ENSP00000418915.1:p.His142=
ENST00000498628.6:c.273T=	ENSP00000467857.1:p.His91=
ENST00000530628.2:c.*27+43T=	ENSP00000432664.2:n.*27+43T=
ENST00000578845.2:c.273T=	ENSP00000467390.1:p.His91=
ENST00000579122.1:c.383+43T=	ENSP00000464202.1:n.383+43T=
ENST00000579755.1:c.*70T=	ENSP00000462950.1:n.*70T=
NM_000077.4:c.426T= , LRG_11t1:c.426T=	NP_000068.1:p.His142=
NM_001195132.1:c.426T=	NP_001182061.1:p.His142=
NM_058195.3:c.*70T= , LRG_11t2:c.*70T=	NP_478102.2:n.*70T=
NM_058197.4:c.700T=	NP_478104.2:n.700T=
XM_005251343.1:c.273T=	XP_005251400.1:p.His91=
XM_011517675.1:c.426T=	XP_011515977.1:p.His142=
XM_011517676.1:c.426T=	XP_011515978.1:p.His142=
XM_011517679.1:c.273T=	XP_011515981.1:p.His91=
XR_929159.1:n.827T=
XR_929161.1:n.616T=
XR_929162.1:n.616T=
XR_929163.1:n.565T=
XR_929164.1:n.348T=
NM_001363763.1:c.273T=	NP_001350692.1:p.His91=
XM_011517675.2:c.426T=	XP_011515977.1:p.His142=
XM_011517676.2:c.426T=	XP_011515978.1:p.His142=
XR_929159.2:n.756T=
NM_001363763.2:c.273T=	NP_001350692.1:p.His91=
NM_000077.5:c.426T= MANE Select	NP_000068.1:p.His142=
NM_001195132.2:c.426T=	NP_001182061.1:p.His142=
NM_058195.4:c.*70T= MANE Plus Clinical	NP_478102.2:n.*70T=
NM_058197.5:c.*349T=	NP_478104.2:n.*349T=