Canonical Allele Identifier: CA479321982

Gene: ALG10B

Linked Data

• MyVariant Identifiers: chr12:g.38712152A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.38318350A>G , CM000674.2:g.38318350A>G	GRCh38
NC_000012.11:g.38712152A>G , CM000674.1:g.38712152A>G	GRCh37
NC_000012.10:g.36998419A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308742.9:c.261A>G MANE Select	ENSP00000310120.4:p.Glu87=
ENST00000308742.8:c.261A>G	ENSP00000310120.4:p.Glu87=
ENST00000548240.1:c.*1A>G	ENSP00000449210.1:n.*1A>G
ENST00000551464.1:c.261A>G	ENSP00000448819.1:p.Glu87=
ENST00000553138.1:n.1584A>G
NM_001013620.3:c.261A>G	NP_001013642.1:p.Glu87=
NM_001308340.1:c.261A>G	NP_001295269.1:p.Glu87=
XM_005268665.3:c.81A>G	XP_005268722.1:p.Glu27=
XM_006719243.2:c.81A>G	XP_006719306.1:p.Glu27=
XM_005268665.4:c.81A>G	XP_005268722.1:p.Glu27=
NM_001013620.4:c.261A>G MANE Select	NP_001013642.2:p.Glu87=
NM_001308340.2:c.261A>G	NP_001295269.2:p.Glu87=