Canonical Allele Identifier: CA480417489

Gene: MDM2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68841626G>C , CM000674.2:g.68841626G>C	GRCh38
NC_000012.11:g.69235406G>C , CM000674.1:g.69235406G>C	GRCh37
NC_000012.10:g.67521673G>C	NCBI36
NG_016708.1:g.38436G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258149.11:c.*1777G>C MANE Select	ENSP00000258149.6:n.*1777G>C
ENST00000258149.10:c.*1777G>C	ENSP00000258149.6:n.*1777G>C
ENST00000258149.9:c.*1777G>C	ENSP00000258149.6:n.*1777G>C
ENST00000356290.8:c.*1777G>C	ENSP00000348637.4:n.*1777G>C
ENST00000462284.5:c.*1777G>C	ENSP00000417281.2:n.*1777G>C
NM_001145337.2:c.*1777G>C	NP_001138809.1:n.*1777G>C
NM_001145339.2:c.*1777G>C	NP_001138811.1:n.*1777G>C
NM_001145340.2:c.*1777G>C	NP_001138812.1:n.*1777G>C
NM_001278462.1:c.*1777G>C	NP_001265391.1:n.*1777G>C
NM_002392.5:c.*1777G>C	NP_002383.2:n.*1777G>C
XM_005268872.5:c.*1777G>C	XP_005268929.1:n.*1777G>C
XM_006719399.4:c.*1777G>C	XP_006719462.1:n.*1777G>C
XM_006719400.4:c.*1777G>C	XP_006719463.1:n.*1777G>C
NM_001145337.3:c.*1777G>C	NP_001138809.1:n.*1777G>C
NM_001145340.3:c.*1777G>C	NP_001138812.1:n.*1777G>C
NM_001278462.2:c.*1777G>C	NP_001265391.1:n.*1777G>C
NM_001367990.1:c.*1777G>C	NP_001354919.1:n.*1777G>C
NM_002392.6:c.*1777G>C MANE Select	NP_002383.2:n.*1777G>C