Canonical Allele Identifier: CA16604411

Gene: MOGS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74465324C>G , CM000664.2:g.74465324C>G	GRCh38
NC_000002.11:g.74692451C>G , CM000664.1:g.74692451C>G	GRCh37
NC_000002.10:g.74545959C>G	NCBI36
NG_008922.1:g.5087G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006302.3:c.-77G>C MANE Select	NP_006293.2:n.-77G>C
ENST00000448666.7:c.-77G>C MANE Select	ENSP00000410992.3:n.-77G>C
NM_001146158.1:c.-69G>C	NP_001139630.1:n.-69G>C
NM_001146158.2:c.-69G>C	NP_001139630.1:n.-69G>C
NM_006302.2:c.-77G>C	NP_006293.2:n.-77G>C
ENST00000233616.8:c.-77G>C	ENSP00000233616.4:n.-77G>C
ENST00000409065.5:c.-77G>C	ENSP00000386493.1:n.-77G>C
ENST00000414701.1:c.-16G>C	ENSP00000396298.1:n.-16G>C
ENST00000448666.5:c.-69G>C	ENSP00000410992.1:n.-69G>C
ENST00000452063.6:c.-69G>C	ENSP00000388201.2:n.-69G>C
ENST00000452063.7:c.-69G>C	ENSP00000388201.2:n.-69G>C
ENST00000462443.1:n.87G>C
ENST00000462443.2:c.-257G>C	ENSP00000497265.1:n.-257G>C
ENST00000486036.1:n.77G>C
ENST00000647753.1:c.-77G>C	ENSP00000497318.1:n.-77G>C
ENST00000647771.1:c.-77G>C	ENSP00000496788.1:n.-77G>C
ENST00000647915.1:c.-69G>C	ENSP00000498123.1:n.-69G>C
ENST00000648768.1:n.4G>C
ENST00000648810.1:c.-202G>C	ENSP00000496949.1:n.-202G>C
ENST00000649075.1:c.-77G>C	ENSP00000497836.1:n.-77G>C
ENST00000649601.1:c.-69G>C	ENSP00000496796.1:n.-69G>C
ENST00000690565.1:c.-77G>C	ENSP00000510501.1:n.-77G>C
ENST00000691308.1:c.-77G>C	ENSP00000509583.1:n.-77G>C