Canonical Allele Identifier: CA347371087

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689178A>G (hg19) ; chr2:g.74462051A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462051A>G , CM000664.2:g.74462051A>G	GRCh38
NC_000002.11:g.74689178A>G , CM000664.1:g.74689178A>G	GRCh37
NC_000002.10:g.74542686A>G	NCBI36
NG_008922.1:g.8360T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1738T>C	ENSP00000510501.1:p.Ser580Pro
ENST00000691308.1:c.958T>C	ENSP00000509583.1:p.Ser320Pro
ENST00000448666.7:c.1738T>C MANE Select	ENSP00000410992.3:p.Ser580Pro
ENST00000452063.7:c.1420T>C	ENSP00000388201.2:p.Ser474Pro
ENST00000462443.2:c.913T>C	ENSP00000497265.1:p.Ser305Pro
ENST00000647723.1:c.1681T>C
ENST00000647753.1:c.*1031T>C	ENSP00000497318.1:n.*1031T>C
ENST00000647771.1:c.*1226T>C	ENSP00000496788.1:n.*1226T>C
ENST00000647915.1:c.*1031T>C	ENSP00000498123.1:n.*1031T>C
ENST00000648768.1:n.1995T>C
ENST00000648810.1:c.913T>C	ENSP00000496949.1:p.Ser305Pro
ENST00000649075.1:c.*666T>C	ENSP00000497836.1:n.*666T>C
ENST00000649601.1:c.*918T>C	ENSP00000496796.1:n.*918T>C
ENST00000649777.1:n.1947T>C
ENST00000649854.1:c.1371T>C
ENST00000233616.8:c.1738T>C	ENSP00000233616.4:p.Ser580Pro
ENST00000409065.5:c.*918T>C	ENSP00000386493.1:n.*918T>C
ENST00000448666.5:c.1420T>C	ENSP00000410992.1:p.Ser474Pro
ENST00000452063.6:c.1420T>C	ENSP00000388201.2:p.Ser474Pro
ENST00000462189.1:n.1419T>C
NM_001146158.1:c.1420T>C	NP_001139630.1:p.Ser474Pro
NM_006302.2:c.1738T>C	NP_006293.2:p.Ser580Pro
NM_006302.3:c.1738T>C MANE Select	NP_006293.2:p.Ser580Pro
NM_001146158.2:c.1420T>C	NP_001139630.1:p.Ser474Pro