Canonical Allele Identifier: CA1839157757

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968091C= , CM000671.2:g.21968091C=	GRCh38
NC_000009.11:g.21968090C= , CM000671.1:g.21968090C=	GRCh37
NC_000009.10:g.21958090C=	NCBI36
NG_007485.1:g.31401G= , LRG_11:g.31401G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.*138G= MANE Select	ENSP00000307101.5:n.*138G=
ENST00000404796.3:c.348-61342C=	ENSP00000385916.2:n.348-61342C=
ENST00000579755.2:c.*253G= MANE Plus Clinical	ENSP00000462950.1:n.*253G=
ENST00000304494.9:c.*138G=	ENSP00000307101.5:n.*138G=
ENST00000361570.4:c.*138G=	ENSP00000355153.4:n.*138G=
ENST00000404796.2:c.348-61342C=	ENSP00000385916.2:n.348-61342C=
ENST00000498124.1:c.*302G=	ENSP00000418915.1:n.*302G=
ENST00000530628.2:c.*179G=	ENSP00000432664.2:n.*179G=
ENST00000578845.2:c.*138G=	ENSP00000467390.1:n.*138G=
ENST00000579122.1:c.*118G=	ENSP00000464202.1:n.*118G=
ENST00000579755.1:c.*253G=	ENSP00000462950.1:n.*253G=
NM_000077.4:c.*138G= , LRG_11t1:c.*138G=	NP_000068.1:n.*138G=
NM_001195132.1:c.*302G=	NP_001182061.1:n.*302G=
NM_058195.3:c.*253G= , LRG_11t2:c.*253G=	NP_478102.2:n.*253G=
NM_058197.4:c.883G=	NP_478104.2:n.883G=
XM_005251343.1:c.*138G=	XP_005251400.1:n.*138G=
XM_011517679.1:c.*138G=	XP_011515981.1:n.*138G=
NM_001363763.1:c.*138G=	NP_001350692.1:n.*138G=
NM_001363763.2:c.*138G=	NP_001350692.1:n.*138G=
NM_000077.5:c.*138G= MANE Select	NP_000068.1:n.*138G=
NM_001195132.2:c.*302G=	NP_001182061.1:n.*302G=
NM_058195.4:c.*253G= MANE Plus Clinical	NP_478102.2:n.*253G=
NM_058197.5:c.*532G=	NP_478104.2:n.*532G=