Canonical Allele Identifier: CA1839173697

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974855C= , CM000671.2:g.21974855C=	GRCh38
NC_000009.11:g.21974854C= , CM000671.1:g.21974854C=	GRCh37
NC_000009.10:g.21964854C=	NCBI36
NG_007485.1:g.24637G= , LRG_11:g.24637G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.-28G= MANE Select	ENSP00000307101.5:n.-28G=
ENST00000404796.3:c.348-54578C=	ENSP00000385916.2:n.348-54578C=
ENST00000579755.2:c.194-3647G= MANE Plus Clinical	ENSP00000462950.1:n.194-3647G=
ENST00000304494.9:c.-28G=	ENSP00000307101.5:n.-28G=
ENST00000361570.4:c.194-3647G=	ENSP00000355153.4:n.194-3647G=
ENST00000404796.2:c.348-54578C=	ENSP00000385916.2:n.348-54578C=
ENST00000494262.5:c.-3-3647G=	ENSP00000464952.1:n.-3-3647G=
ENST00000498124.1:c.-28G=	ENSP00000418915.1:n.-28G=
ENST00000498628.6:c.-3-3647G=	ENSP00000467857.1:n.-3-3647G=
ENST00000530628.2:c.194-3647G=	ENSP00000432664.2:n.194-3647G=
ENST00000579122.1:c.-28G=	ENSP00000464202.1:n.-28G=
ENST00000579755.1:c.194-3647G=	ENSP00000462950.1:n.194-3647G=
NM_000077.4:c.-28G= , LRG_11t1:c.-28G=	NP_000068.1:n.-28G=
NM_001195132.1:c.-28G=	NP_001182061.1:n.-28G=
NM_058195.3:c.194-3647G= , LRG_11t2:c.194-3647G=	NP_478102.2:n.194-3647G=
XM_011517675.1:c.-28G=	XP_011515977.1:n.-28G=
XM_011517676.1:c.-28G=	XP_011515978.1:n.-28G=
XM_011517679.1:c.-3-3647G=	XP_011515981.1:n.-3-3647G=
XR_929159.1:n.374G=
XR_929161.1:n.341-3647G=
XR_929162.1:n.341-3647G=
XR_929163.1:n.290-3647G=
NM_001363763.1:c.-3-3647G=	NP_001350692.1:n.-3-3647G=
XM_011517675.2:c.-28G=	XP_011515977.1:n.-28G=
XM_011517676.2:c.-28G=	XP_011515978.1:n.-28G=
XR_929159.2:n.303G=
NM_001363763.2:c.-3-3647G=	NP_001350692.1:n.-3-3647G=
NM_000077.5:c.-28G= MANE Select	NP_000068.1:n.-28G=
NM_001195132.2:c.-28G=	NP_001182061.1:n.-28G=
NM_058195.4:c.194-3647G= MANE Plus Clinical	NP_478102.2:n.194-3647G=
NM_058197.5:c.-28G=	NP_478104.2:n.-28G=