Canonical Allele Identifier: CA9774866

Linked Data

ClinVar Variation Id: 380041
ClinVar RCV Id: RCV001775792
dbSNP Id: rs11551768

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.17969902A>T , CM000682.2:g.17969902A>T GRCh38
NC_000020.10:g.17950545A>T , CM000682.1:g.17950545A>T GRCh37
NC_000020.9:g.17898545A>T NCBI36
NG_042236.1:g.6012A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377710.10:c.43A>T (MGME1) MANE Select ENSP00000366939.5:p.Ser15Cys
ENST00000377704.4:c.43A>T (MGME1) ENSP00000366933.4:p.Ser15Cys
ENST00000377709.1:c.43A>T (MGME1) ENSP00000366938.1:p.Ser15Cys
ENST00000377710.9:c.43A>T (MGME1) ENSP00000366939.5:p.Ser15Cys
ENST00000486776.5:n.492-12865T>A (OVOL2)
NM_001310338.1:c.43A>T (MGME1) NP_001297267.1:p.Ser15Cys
NM_001310339.1:c.43A>T (MGME1) NP_001297268.1:p.Ser15Cys
NM_052865.2:c.43A>T (MGME1) NP_443097.1:p.Ser15Cys
NM_052865.3:c.43A>T (MGME1) NP_443097.1:p.Ser15Cys
XM_005260867.2:c.43A>T (MGME1) XP_005260924.1:p.Ser15Cys
XM_005260870.2:c.43A>T (MGME1) XP_005260927.1:p.Ser15Cys
XM_006723663.2:c.43A>T (MGME1) XP_006723726.1:p.Ser15Cys
XM_011529394.1:c.43A>T (MGME1) XP_011527696.1:p.Ser15Cys
XM_011529395.1:c.43A>T (MGME1) XP_011527697.1:p.Ser15Cys
NM_001363738.1:c.43A>T (MGME1) NP_001350667.1:p.Ser15Cys
XM_005260867.3:c.43A>T (MGME1) XP_005260924.1:p.Ser15Cys
XM_005260870.4:c.43A>T (MGME1) XP_005260927.1:p.Ser15Cys
XM_006723663.4:c.43A>T (MGME1) XP_006723726.1:p.Ser15Cys
XM_017028127.2:c.43A>T (MGME1) XP_016883616.1:p.Ser15Cys
XM_017028128.1:c.43A>T (MGME1) XP_016883617.1:p.Ser15Cys
XM_024452017.1:c.43A>T (MGME1) XP_024307785.1:p.Ser15Cys
NM_052865.4:c.43A>T (MGME1) MANE Select NP_443097.1:p.Ser15Cys
NM_001310338.2:c.43A>T (MGME1) NP_001297267.1:p.Ser15Cys
NM_001310339.2:c.43A>T (MGME1) NP_001297268.1:p.Ser15Cys
NM_001363738.2:c.43A>T (MGME1) NP_001350667.1:p.Ser15Cys