Canonical Allele Identifier: CA1839173702

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974856T= , CM000671.2:g.21974856T=	GRCh38
NC_000009.11:g.21974855T= , CM000671.1:g.21974855T=	GRCh37
NC_000009.10:g.21964855T=	NCBI36
NG_007485.1:g.24636A= , LRG_11:g.24636A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.-29A= MANE Select	ENSP00000307101.5:n.-29A=
ENST00000404796.3:c.348-54577T=	ENSP00000385916.2:n.348-54577T=
ENST00000579755.2:c.194-3648A= MANE Plus Clinical	ENSP00000462950.1:n.194-3648A=
ENST00000304494.9:c.-29A=	ENSP00000307101.5:n.-29A=
ENST00000361570.4:c.194-3648A=	ENSP00000355153.4:n.194-3648A=
ENST00000404796.2:c.348-54577T=	ENSP00000385916.2:n.348-54577T=
ENST00000494262.5:c.-3-3648A=	ENSP00000464952.1:n.-3-3648A=
ENST00000498124.1:c.-29A=	ENSP00000418915.1:n.-29A=
ENST00000498628.6:c.-3-3648A=	ENSP00000467857.1:n.-3-3648A=
ENST00000530628.2:c.194-3648A=	ENSP00000432664.2:n.194-3648A=
ENST00000579122.1:c.-29A=	ENSP00000464202.1:n.-29A=
ENST00000579755.1:c.194-3648A=	ENSP00000462950.1:n.194-3648A=
NM_000077.4:c.-29A= , LRG_11t1:c.-29A=	NP_000068.1:n.-29A=
NM_001195132.1:c.-29A=	NP_001182061.1:n.-29A=
NM_058195.3:c.194-3648A= , LRG_11t2:c.194-3648A=	NP_478102.2:n.194-3648A=
XM_011517675.1:c.-29A=	XP_011515977.1:n.-29A=
XM_011517676.1:c.-29A=	XP_011515978.1:n.-29A=
XM_011517679.1:c.-3-3648A=	XP_011515981.1:n.-3-3648A=
XR_929159.1:n.373A=
XR_929161.1:n.341-3648A=
XR_929162.1:n.341-3648A=
XR_929163.1:n.290-3648A=
NM_001363763.1:c.-3-3648A=	NP_001350692.1:n.-3-3648A=
XM_011517675.2:c.-29A=	XP_011515977.1:n.-29A=
XM_011517676.2:c.-29A=	XP_011515978.1:n.-29A=
XR_929159.2:n.302A=
NM_001363763.2:c.-3-3648A=	NP_001350692.1:n.-3-3648A=
NM_000077.5:c.-29A= MANE Select	NP_000068.1:n.-29A=
NM_001195132.2:c.-29A=	NP_001182061.1:n.-29A=
NM_058195.4:c.194-3648A= MANE Plus Clinical	NP_478102.2:n.194-3648A=
NM_058197.5:c.-29A=	NP_478104.2:n.-29A=