Canonical Allele Identifier: CA1839173836

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974924C= , CM000671.2:g.21974924C=	GRCh38
NC_000009.11:g.21974923C= , CM000671.1:g.21974923C=	GRCh37
NC_000009.10:g.21964923C=	NCBI36
NG_007485.1:g.24568G= , LRG_11:g.24568G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-54509C=	ENSP00000385916.2:n.348-54509C=
ENST00000579755.2:c.194-3716G= MANE Plus Clinical	ENSP00000462950.1:n.194-3716G=
ENST00000304494.9:c.-97G=	ENSP00000307101.5:n.-97G=
ENST00000361570.4:c.194-3716G=	ENSP00000355153.4:n.194-3716G=
ENST00000404796.2:c.348-54509C=	ENSP00000385916.2:n.348-54509C=
ENST00000494262.5:c.-3-3716G=	ENSP00000464952.1:n.-3-3716G=
ENST00000498628.6:c.-3-3716G=	ENSP00000467857.1:n.-3-3716G=
ENST00000530628.2:c.194-3716G=	ENSP00000432664.2:n.194-3716G=
ENST00000579755.1:c.194-3716G=	ENSP00000462950.1:n.194-3716G=
NM_000077.4:c.-97G= , LRG_11t1:c.-97G=	NP_000068.1:n.-97G=
NM_001195132.1:c.-97G=	NP_001182061.1:n.-97G=
NM_058195.3:c.194-3716G= , LRG_11t2:c.194-3716G=	NP_478102.2:n.194-3716G=
XM_011517675.1:c.-97G=	XP_011515977.1:n.-97G=
XM_011517676.1:c.-97G=	XP_011515978.1:n.-97G=
XM_011517679.1:c.-3-3716G=	XP_011515981.1:n.-3-3716G=
XR_929159.1:n.305G=
XR_929161.1:n.341-3716G=
XR_929162.1:n.341-3716G=
XR_929163.1:n.290-3716G=
NM_001363763.1:c.-3-3716G=	NP_001350692.1:n.-3-3716G=
XM_011517675.2:c.-97G=	XP_011515977.1:n.-97G=
XM_011517676.2:c.-97G=	XP_011515978.1:n.-97G=
XR_929159.2:n.234G=
NM_001363763.2:c.-3-3716G=	NP_001350692.1:n.-3-3716G=
NM_058195.4:c.194-3716G= MANE Plus Clinical	NP_478102.2:n.194-3716G=