Canonical Allele Identifier: CA384575573

Gene: ALG10B

Linked Data

• MyVariant Identifiers: chr12:g.38712146G>T (hg19) ; chr12:g.38318344G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.38318344G>T , CM000674.2:g.38318344G>T	GRCh38
NC_000012.11:g.38712146G>T , CM000674.1:g.38712146G>T	GRCh37
NC_000012.10:g.36998413G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000308742.9:c.255G>T MANE Select	ENSP00000310120.4:p.Trp85Cys
ENST00000308742.8:c.255G>T	ENSP00000310120.4:p.Trp85Cys
ENST00000548240.1:c.229G>T	ENSP00000449210.1:p.Val77Phe
ENST00000551464.1:c.255G>T	ENSP00000448819.1:p.Trp85Cys
ENST00000553138.1:n.1578G>T
NM_001013620.3:c.255G>T	NP_001013642.1:p.Trp85Cys
NM_001308340.1:c.255G>T	NP_001295269.1:p.Trp85Cys
XM_005268665.3:c.75G>T	XP_005268722.1:p.Trp25Cys
XM_006719243.2:c.75G>T	XP_006719306.1:p.Trp25Cys
XM_005268665.4:c.75G>T	XP_005268722.1:p.Trp25Cys
NM_001013620.4:c.255G>T MANE Select	NP_001013642.2:p.Trp85Cys
NM_001308340.2:c.255G>T	NP_001295269.2:p.Trp85Cys