Canonical Allele Identifier: CA2044139153
Gene: MDM2 HGNC NCBI

Linked Data

dbSNP Id: rs1880594205

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68808791_68808798dup , CM000674.2:g.68808791_68808798dup GRCh38
NC_000012.11:g.69202571_69202578dup , CM000674.1:g.69202571_69202578dup GRCh37
NC_000012.10:g.67488838_67488845dup NCBI36
NG_016708.1:g.5601_5608dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000258149.11:c.14+300_14+307dup MANE Select ENSP00000258149.6:n.14+300_14+307dup
ENST00000258149.10:c.14+300_14+307dup ENSP00000258149.6:n.14+300_14+307dup
ENST00000393417.8:c.14+300_14+307dup ENSP00000429021.3:n.14+300_14+307dup
ENST00000258148.11:c.14+300_14+307dup ENSP00000258148.7:n.14+300_14+307dup
ENST00000258149.9:c.14+300_14+307dup ENSP00000258149.6:n.14+300_14+307dup
ENST00000311420.13:c.14+300_14+307dup ENSP00000310742.9:n.14+300_14+307dup
ENST00000393412.7:c.-5+300_-5+307dup ENSP00000377064.4:n.-5+300_-5+307dup
ENST00000393417.7:c.-5+300_-5+307dup ENSP00000429021.2:n.-5+300_-5+307dup
ENST00000428863.6:c.-5+300_-5+307dup ENSP00000410694.3:n.-5+300_-5+307dup
ENST00000462284.5:c.-5+300_-5+307dup ENSP00000417281.2:n.-5+300_-5+307dup
ENST00000493419.1:n.210+300_210+307dup
NM_001145339.2:c.14+300_14+307dup NP_001138811.1:n.14+300_14+307dup
NM_002392.5:c.14+300_14+307dup NP_002383.2:n.14+300_14+307dup
XM_006719400.2:c.-174+300_-174+307dup XP_006719463.1:n.-174+300_-174+307dup
XM_005268872.5:c.-300_-293dup XP_005268929.1:n.-300_-293dup
XM_006719400.4:c.-174+300_-174+307dup XP_006719463.1:n.-174+300_-174+307dup
NM_002392.6:c.14+300_14+307dup MANE Select NP_002383.2:n.14+300_14+307dup