Canonical Allele Identifier: CA479321975

Gene: ALG10B

Linked Data

• MyVariant Identifiers: chr12:g.38712143A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.38318341A>T , CM000674.2:g.38318341A>T	GRCh38
NC_000012.11:g.38712143A>T , CM000674.1:g.38712143A>T	GRCh37
NC_000012.10:g.36998410A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308742.9:c.252A>T MANE Select	ENSP00000310120.4:p.Ala84=
ENST00000308742.8:c.252A>T	ENSP00000310120.4:p.Ala84=
ENST00000548240.1:c.226A>T	ENSP00000449210.1:p.Met76Leu
ENST00000551464.1:c.252A>T	ENSP00000448819.1:p.Ala84=
ENST00000553138.1:n.1575A>T
NM_001013620.3:c.252A>T	NP_001013642.1:p.Gly84=
NM_001308340.1:c.252A>T	NP_001295269.1:p.Gly84=
XM_005268665.3:c.72A>T	XP_005268722.1:p.Ala24=
XM_006719243.2:c.72A>T	XP_006719306.1:p.Ala24=
XM_005268665.4:c.72A>T	XP_005268722.1:p.Ala24=
NM_001013620.4:c.252A>T MANE Select	NP_001013642.2:p.Ala84=
NM_001308340.2:c.252A>T	NP_001295269.2:p.Ala84=