Canonical Allele Identifier: CA730383630

Gene: MDM4

Linked Data

• dbSNP Id: rs1455417512
• gnomAD v4: 1-204556364-G-A
• MyVariant Identifiers: chr1:g.204525492G>A (hg19) ; chr1:g.204556364G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204556364G>A , CM000663.2:g.204556364G>A	GRCh38
NC_000001.10:g.204525492G>A , CM000663.1:g.204525492G>A	GRCh37
NC_000001.9:g.202792115G>A	NCBI36
NG_029367.1:g.44986G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367182.8:c.*6682G>A MANE Select	ENSP00000356150.3:n.*6682G>A
ENST00000367182.7:c.*6682G>A	ENSP00000356150.3:n.*6682G>A
ENST00000367183.7:c.*6682G>A	ENSP00000356151.3:n.*6682G>A
ENST00000391947.6:c.*7664G>A	ENSP00000375811.2:n.*7664G>A
ENST00000454264.6:c.*6682G>A	ENSP00000396840.2:n.*6682G>A
ENST00000612738.4:c.*6682G>A	ENSP00000478080.1:n.*6682G>A
ENST00000614459.4:c.*6682G>A	ENSP00000482388.1:n.*6682G>A
ENST00000616250.4:c.*7325G>A	ENSP00000478581.1:n.*7325G>A
NM_001204171.1:c.*6682G>A	NP_001191100.1:n.*6682G>A
NM_001204172.1:c.*6682G>A	NP_001191101.1:n.*6682G>A
NM_001278516.1:c.*7664G>A	NP_001265445.1:n.*7664G>A
NM_001278517.1:c.*6682G>A	NP_001265446.1:n.*6682G>A
NM_001278518.1:c.*7325G>A	NP_001265447.1:n.*7325G>A
NM_001278519.1:c.*6682G>A	NP_001265448.1:n.*6682G>A
NM_002393.4:c.*6682G>A	NP_002384.2:n.*6682G>A
XM_011509565.1:c.954-2277G>A	XP_011507867.1:n.954-2277G>A
NM_002393.5:c.*6682G>A MANE Select	NP_002384.2:n.*6682G>A
NM_001204171.2:c.*6682G>A	NP_001191100.1:n.*6682G>A
NM_001204172.2:c.*6682G>A	NP_001191101.1:n.*6682G>A
NM_001278516.2:c.*7664G>A	NP_001265445.1:n.*7664G>A
NM_001278517.2:c.*6682G>A	NP_001265446.1:n.*6682G>A
NM_001278518.2:c.*7325G>A	NP_001265447.1:n.*7325G>A
NM_001278519.2:c.*6682G>A	NP_001265448.1:n.*6682G>A