Canonical Allele Identifier: CA2044138878

Gene: MDM2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68808384A= , CM000674.2:g.68808384A=	GRCh38
NC_000012.11:g.69202164A= , CM000674.1:g.69202164A=	GRCh37
NC_000012.10:g.67488431A=	NCBI36
NG_016708.1:g.5194A=

Transcript Alleles

HGVS	Amino-acid Change
NM_002392.6:c.-94A= MANE Select	NP_002383.2:n.-94A=
ENST00000258149.11:c.-94A= MANE Select	ENSP00000258149.6:n.-94A=
NM_001145339.2:c.-94A=	NP_001138811.1:n.-94A=
NM_002392.5:c.-94A=	NP_002383.2:n.-94A=
ENST00000258149.10:c.-94A=	ENSP00000258149.6:n.-94A=
ENST00000258149.9:c.-94A=	ENSP00000258149.6:n.-94A=
ENST00000311420.13:c.-94A=	ENSP00000310742.9:n.-94A=
ENST00000393412.7:c.-112A=	ENSP00000377064.4:n.-112A=
ENST00000393417.7:c.-112A=	ENSP00000429021.2:n.-112A=
ENST00000393417.8:c.-94A=	ENSP00000429021.3:n.-94A=
ENST00000428863.6:c.-112A=	ENSP00000410694.3:n.-112A=
ENST00000462284.5:c.-112A=	ENSP00000417281.2:n.-112A=
ENST00000493419.1:n.103A=
XM_006719400.2:c.-281A=	XP_006719463.1:n.-281A=
XM_006719400.4:c.-281A=	XP_006719463.1:n.-281A=