Canonical Allele Identifier: CA12229623

Gene: MOG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672244T>C , CM000668.2:g.29672244T>C	GRCh38
NC_000006.11:g.29640021T>C , CM000668.1:g.29640021T>C	GRCh37
NC_000006.10:g.29748000T>C	NCBI36
NG_013045.1:g.9911A>G
NG_031873.1:g.20264T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_206809.4:c.*1059T>C MANE Select	NP_996532.2:n.*1059T>C
ENST00000376917.8:c.*1059T>C MANE Select	ENSP00000366115.3:n.*1059T>C
NM_001008228.2:c.*1059T>C	NP_001008229.1:n.*1059T>C
NM_001008228.3:c.*1059T>C	NP_001008229.1:n.*1059T>C
NM_001008229.2:c.*794T>C	NP_001008230.1:n.*794T>C
NM_001008229.3:c.*794T>C	NP_001008230.1:n.*794T>C
NM_001170418.1:c.*1059T>C	NP_001163889.1:n.*1059T>C
NM_001170418.2:c.*1059T>C	NP_001163889.1:n.*1059T>C
NM_001363610.1:c.*1365T>C	NP_001350539.1:n.*1365T>C
NM_001363610.2:c.*1365T>C	NP_001350539.1:n.*1365T>C
NM_002433.4:c.*794T>C	NP_002424.3:n.*794T>C
NM_002433.5:c.*794T>C	NP_002424.3:n.*794T>C
NM_206809.3:c.*1059T>C	NP_996532.2:n.*1059T>C
NM_206810.3:c.*794T>C	NP_996533.2:n.*794T>C
NM_206810.4:c.*794T>C	NP_996533.2:n.*794T>C
NM_206811.3:c.*794T>C	NP_996534.2:n.*794T>C
NM_206811.4:c.*794T>C	NP_996534.2:n.*794T>C
NM_206812.3:c.*1059T>C	NP_996535.2:n.*1059T>C
NM_206812.4:c.*1059T>C	NP_996535.2:n.*1059T>C
NM_206814.5:c.*1059T>C	NP_996537.3:n.*1059T>C
NM_206814.6:c.*1059T>C	NP_996537.3:n.*1059T>C
ENST00000376889.3:c.1853T>C
ENST00000376894.8:c.*1365T>C	ENSP00000366091.4:n.*1365T>C
ENST00000376917.7:c.*1059T>C	ENSP00000366115.3:n.*1059T>C
ENST00000431798.6:c.1686T>C	ENSP00000410866.2:n.1686T>C