Canonical Allele Identifier: CA479321980

Gene: ALG10B

Linked Data

• MyVariant Identifiers: chr12:g.38712149T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.38318347T>C , CM000674.2:g.38318347T>C	GRCh38
NC_000012.11:g.38712149T>C , CM000674.1:g.38712149T>C	GRCh37
NC_000012.10:g.36998416T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000308742.9:c.258T>C MANE Select	ENSP00000310120.4:p.Ser86=
ENST00000308742.8:c.258T>C	ENSP00000310120.4:p.Ser86=
ENST00000548240.1:c.232T>C	ENSP00000449210.1:p.Ter78Arg
ENST00000551464.1:c.258T>C	ENSP00000448819.1:p.Ser86=
ENST00000553138.1:n.1581T>C
NM_001013620.3:c.258T>C	NP_001013642.1:p.Ser86=
NM_001308340.1:c.258T>C	NP_001295269.1:p.Ser86=
XM_005268665.3:c.78T>C	XP_005268722.1:p.Ser26=
XM_006719243.2:c.78T>C	XP_006719306.1:p.Ser26=
XM_005268665.4:c.78T>C	XP_005268722.1:p.Ser26=
NM_001013620.4:c.258T>C MANE Select	NP_001013642.2:p.Ser86=
NM_001308340.2:c.258T>C	NP_001295269.2:p.Ser86=