Canonical Allele Identifier: CA384575392

Gene: ALG10B

Linked Data

• MyVariant Identifiers: chr12:g.38712062G>T (hg19) ; chr12:g.38318260G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.38318260G>T , CM000674.2:g.38318260G>T	GRCh38
NC_000012.11:g.38712062G>T , CM000674.1:g.38712062G>T	GRCh37
NC_000012.10:g.36998329G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308742.9:c.172-1G>T MANE Select	ENSP00000310120.4:n.172-1G>T
ENST00000308742.8:c.172-1G>T	ENSP00000310120.4:n.172-1G>T
ENST00000548240.1:c.146-1G>T	ENSP00000449210.1:n.146-1G>T
ENST00000551464.1:c.172-1G>T	ENSP00000448819.1:n.172-1G>T
ENST00000553138.1:n.1494G>T
NM_001013620.3:c.172-1G>T	NP_001013642.1:n.172-1G>T
NM_001308340.1:c.172-1G>T	NP_001295269.1:n.172-1G>T
XM_005268665.3:c.-9-1G>T	XP_005268722.1:n.-9-1G>T
XM_006719243.2:c.-9-1G>T	XP_006719306.1:n.-9-1G>T
XM_005268665.4:c.-9-1G>T	XP_005268722.1:n.-9-1G>T
NM_001013620.4:c.172-1G>T MANE Select	NP_001013642.2:n.172-1G>T
NM_001308340.2:c.172-1G>T	NP_001295269.2:n.172-1G>T