Canonical Allele Identifier: CA691319206

Gene: MDM2

Linked Data

• dbSNP Id: rs1272817927
• MyVariant Identifiers: chr12:g.69202399_69202419del (hg19) ; chr12:g.68808619_68808639del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68808622_68808642del , CM000674.2:g.68808622_68808642del	GRCh38
NC_000012.11:g.69202402_69202422del , CM000674.1:g.69202402_69202422del	GRCh37
NC_000012.10:g.67488669_67488689del	NCBI36
NG_016708.1:g.5432_5452del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258149.11:c.14+131_14+151del MANE Select	ENSP00000258149.6:n.14+131_14+151del
ENST00000258149.10:c.14+131_14+151del	ENSP00000258149.6:n.14+131_14+151del
ENST00000393417.8:c.14+131_14+151del	ENSP00000429021.3:n.14+131_14+151del
ENST00000258148.11:c.14+131_14+151del	ENSP00000258148.7:n.14+131_14+151del
ENST00000258149.9:c.14+131_14+151del	ENSP00000258149.6:n.14+131_14+151del
ENST00000311420.13:c.14+131_14+151del	ENSP00000310742.9:n.14+131_14+151del
ENST00000393412.7:c.-5+131_-5+151del	ENSP00000377064.4:n.-5+131_-5+151del
ENST00000393417.7:c.-5+131_-5+151del	ENSP00000429021.2:n.-5+131_-5+151del
ENST00000428863.6:c.-5+131_-5+151del	ENSP00000410694.3:n.-5+131_-5+151del
ENST00000462284.5:c.-5+131_-5+151del	ENSP00000417281.2:n.-5+131_-5+151del
ENST00000493419.1:n.210+131_210+151del
NM_001145339.2:c.14+131_14+151del	NP_001138811.1:n.14+131_14+151del
NM_002392.5:c.14+131_14+151del	NP_002383.2:n.14+131_14+151del
XM_006719400.2:c.-174+131_-174+151del	XP_006719463.1:n.-174+131_-174+151del
XM_006719400.4:c.-174+131_-174+151del	XP_006719463.1:n.-174+131_-174+151del
NM_002392.6:c.14+131_14+151del MANE Select	NP_002383.2:n.14+131_14+151del