Canonical Allele Identifier: CA2410564863

Gene: ALG12

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49913660_49913663delinsTCTC , CM000684.2:g.49913660_49913663delinsTCTC	GRCh38
NC_000022.10:g.50307308_50307311delinsTCTC , CM000684.1:g.50307308_50307311delinsTCTC	GRCh37
NC_000022.9:g.48693312_48693315delinsTCTC	NCBI36
NG_008927.1:g.9796_9799delinsGAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.103_106delinsGAGA MANE Select	ENSP00000333813.5:p.Glu35=
ENST00000330817.10:c.103_106delinsGAGA	ENSP00000333813.5:p.Glu35=
NM_024105.3:c.103_106delinsGAGA	NP_077010.1:p.Glu35=
XM_011530369.1:c.103_106delinsGAGA	XP_011528671.1:p.Glu35=
XM_011530370.1:c.103_106delinsGAGA	XP_011528672.1:p.Glu35=
XM_011530371.1:c.103_106delinsGAGA	XP_011528673.1:p.Glu35=
XM_011530371.2:c.103_106delinsGAGA	XP_011528673.1:p.Glu35=
XM_017028936.1:c.103_106delinsGAGA	XP_016884425.1:p.Glu35=
XM_017028937.1:c.103_106delinsGAGA	XP_016884426.1:p.Glu35=
NM_024105.4:c.103_106delinsGAGA MANE Select	NP_077010.1:p.Glu35=