Canonical Allele Identifier: CA347371925

Gene: MOGS

Linked Data

• MyVariant Identifiers: chr2:g.74689364G>A (hg19) ; chr2:g.74462237G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74462237G>A , CM000664.2:g.74462237G>A	GRCh38
NC_000002.11:g.74689364G>A , CM000664.1:g.74689364G>A	GRCh37
NC_000002.10:g.74542872G>A	NCBI36
NG_008922.1:g.8174C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690565.1:c.1552C>T	ENSP00000510501.1:p.Pro518Ser
ENST00000691308.1:c.829-57C>T	ENSP00000509583.1:n.829-57C>T
ENST00000448666.7:c.1552C>T MANE Select	ENSP00000410992.3:p.Pro518Ser
ENST00000452063.7:c.1234C>T	ENSP00000388201.2:p.Pro412Ser
ENST00000462443.2:c.727C>T	ENSP00000497265.1:p.Pro243Ser
ENST00000647723.1:c.1495C>T
ENST00000647753.1:c.*845C>T	ENSP00000497318.1:n.*845C>T
ENST00000647771.1:c.*1040C>T	ENSP00000496788.1:n.*1040C>T
ENST00000647915.1:c.*845C>T	ENSP00000498123.1:n.*845C>T
ENST00000648768.1:n.1809C>T
ENST00000648810.1:c.727C>T	ENSP00000496949.1:p.Pro243Ser
ENST00000649075.1:c.*480C>T	ENSP00000497836.1:n.*480C>T
ENST00000649601.1:c.*732C>T	ENSP00000496796.1:n.*732C>T
ENST00000649777.1:n.1761C>T
ENST00000649854.1:c.1185C>T
ENST00000233616.8:c.1552C>T	ENSP00000233616.4:p.Pro518Ser
ENST00000409065.5:c.*732C>T	ENSP00000386493.1:n.*732C>T
ENST00000448666.5:c.1234C>T	ENSP00000410992.1:p.Pro412Ser
ENST00000452063.6:c.1234C>T	ENSP00000388201.2:p.Pro412Ser
ENST00000462189.1:n.1233C>T
NM_001146158.1:c.1234C>T	NP_001139630.1:p.Pro412Ser
NM_006302.2:c.1552C>T	NP_006293.2:p.Pro518Ser
NM_006302.3:c.1552C>T MANE Select	NP_006293.2:p.Pro518Ser
NM_001146158.2:c.1234C>T	NP_001139630.1:p.Pro412Ser