Canonical Allele Identifier: CA2030022486

Gene: ALG10B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.38318238_38318248delinsCTTCATTTTCT , CM000674.2:g.38318238_38318248delinsCTTCATTTTCT	GRCh38
NC_000012.11:g.38712040_38712050delinsCTTCATTTTCT , CM000674.1:g.38712040_38712050delinsCTTCATTTTCT	GRCh37
NC_000012.10:g.36998307_36998317delinsCTTCATTTTCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308742.9:c.172-23_172-13delinsCTTCATTTTCT MANE Select	ENSP00000310120.4:n.172-23_172-13delinsCTTCATTTTCT
ENST00000308742.8:c.172-23_172-13delinsCTTCATTTTCT	ENSP00000310120.4:n.172-23_172-13delinsCTTCATTTTCT
ENST00000548240.1:c.146-23_146-13delinsCTTCATTTTCT	ENSP00000449210.1:n.146-23_146-13delinsCTTCATTTTCT
ENST00000551464.1:c.172-23_172-13delinsCTTCATTTTCT	ENSP00000448819.1:n.172-23_172-13delinsCTTCATTTTCT
ENST00000553138.1:n.1472_1482delinsCTTCATTTTCT
NM_001013620.3:c.172-23_172-13delinsCTTCATTTTCT	NP_001013642.1:n.172-23_172-13delinsCTTCATTTTCT
NM_001308340.1:c.172-23_172-13delinsCTTCATTTTCT	NP_001295269.1:n.172-23_172-13delinsCTTCATTTTCT
XM_005268665.3:c.-9-23_-9-13delinsCTTCATTTTCT	XP_005268722.1:n.-9-23_-9-13delinsCTTCATTTTCT
XM_006719243.2:c.-9-23_-9-13delinsCTTCATTTTCT	XP_006719306.1:n.-9-23_-9-13delinsCTTCATTTTCT
XM_005268665.4:c.-9-23_-9-13delinsCTTCATTTTCT	XP_005268722.1:n.-9-23_-9-13delinsCTTCATTTTCT
NM_001013620.4:c.172-23_172-13delinsCTTCATTTTCT MANE Select	NP_001013642.2:n.172-23_172-13delinsCTTCATTTTCT
NM_001308340.2:c.172-23_172-13delinsCTTCATTTTCT	NP_001295269.2:n.172-23_172-13delinsCTTCATTTTCT