Canonical Allele Identifier: CA2410564859

Gene: ALG12

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49913648_49913649delinsGC , CM000684.2:g.49913648_49913649delinsGC	GRCh38
NC_000022.10:g.50307296_50307297delinsGC , CM000684.1:g.50307296_50307297delinsGC	GRCh37
NC_000022.9:g.48693300_48693301delinsGC	NCBI36
NG_008927.1:g.9810_9811delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.117_118delinsGC MANE Select	ENSP00000333813.5:p.Leu39=
ENST00000330817.10:c.117_118delinsGC	ENSP00000333813.5:p.Leu39=
NM_024105.3:c.117_118delinsGC	NP_077010.1:p.Leu39=
XM_011530369.1:c.117_118delinsGC	XP_011528671.1:p.Leu39=
XM_011530370.1:c.117_118delinsGC	XP_011528672.1:p.Leu39=
XM_011530371.1:c.117_118delinsGC	XP_011528673.1:p.Leu39=
XM_011530371.2:c.117_118delinsGC	XP_011528673.1:p.Leu39=
XM_017028936.1:c.117_118delinsGC	XP_016884425.1:p.Leu39=
XM_017028937.1:c.117_118delinsGC	XP_016884426.1:p.Leu39=
NM_024105.4:c.117_118delinsGC MANE Select	NP_077010.1:p.Leu39=