Canonical Allele Identifier: CA427034030

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689362A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462235A>T , CM000664.2:g.74462235A>T	GRCh38
NC_000002.11:g.74689362A>T , CM000664.1:g.74689362A>T	GRCh37
NC_000002.10:g.74542870A>T	NCBI36
NG_008922.1:g.8176T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1554T>A	ENSP00000510501.1:p.Pro518=
ENST00000691308.1:c.829-55T>A	ENSP00000509583.1:n.829-55T>A
ENST00000448666.7:c.1554T>A MANE Select	ENSP00000410992.3:p.Pro518=
ENST00000452063.7:c.1236T>A	ENSP00000388201.2:p.Pro412=
ENST00000462443.2:c.729T>A	ENSP00000497265.1:p.Pro243=
ENST00000647723.1:c.1497T>A
ENST00000647753.1:c.*847T>A	ENSP00000497318.1:n.*847T>A
ENST00000647771.1:c.*1042T>A	ENSP00000496788.1:n.*1042T>A
ENST00000647915.1:c.*847T>A	ENSP00000498123.1:n.*847T>A
ENST00000648768.1:n.1811T>A
ENST00000648810.1:c.729T>A	ENSP00000496949.1:p.Pro243=
ENST00000649075.1:c.*482T>A	ENSP00000497836.1:n.*482T>A
ENST00000649601.1:c.*734T>A	ENSP00000496796.1:n.*734T>A
ENST00000649777.1:n.1763T>A
ENST00000649854.1:c.1187T>A
ENST00000233616.8:c.1554T>A	ENSP00000233616.4:p.Pro518=
ENST00000409065.5:c.*734T>A	ENSP00000386493.1:n.*734T>A
ENST00000448666.5:c.1236T>A	ENSP00000410992.1:p.Pro412=
ENST00000452063.6:c.1236T>A	ENSP00000388201.2:p.Pro412=
ENST00000462189.1:n.1235T>A
NM_001146158.1:c.1236T>A	NP_001139630.1:p.Pro412=
NM_006302.2:c.1554T>A	NP_006293.2:p.Pro518=
NM_006302.3:c.1554T>A MANE Select	NP_006293.2:p.Pro518=
NM_001146158.2:c.1236T>A	NP_001139630.1:p.Pro412=