Canonical Allele Identifier: CA2410562569

Gene: ALG12

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49909242_49909243delinsAC , CM000684.2:g.49909242_49909243delinsAC	GRCh38
NC_000022.10:g.50302890_50302891delinsAC , CM000684.1:g.50302890_50302891delinsAC	GRCh37
NC_000022.9:g.48688894_48688895delinsAC	NCBI36
NG_008927.1:g.14216_14217delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.768+1_768+2delinsGT MANE Select	ENSP00000333813.5:n.768+1_768+2delinsGT
ENST00000330817.10:c.768+1_768+2delinsGT	ENSP00000333813.5:n.768+1_768+2delinsGT
ENST00000492791.1:c.299+1_299+2delinsGT
NM_024105.3:c.768+1_768+2delinsGT	NP_077010.1:n.768+1_768+2delinsGT
XM_011530369.1:c.768+1_768+2delinsGT	XP_011528671.1:n.768+1_768+2delinsGT
XM_011530370.1:c.768+1_768+2delinsGT	XP_011528672.1:n.768+1_768+2delinsGT
XM_011530371.1:c.768+1_768+2delinsGT	XP_011528673.1:n.768+1_768+2delinsGT
XM_011530371.2:c.768+1_768+2delinsGT	XP_011528673.1:n.768+1_768+2delinsGT
XM_017028936.1:c.768+1_768+2delinsGT	XP_016884425.1:n.768+1_768+2delinsGT
XM_017028937.1:c.768+1_768+2delinsGT	XP_016884426.1:n.768+1_768+2delinsGT
NM_024105.4:c.768+1_768+2delinsGT MANE Select	NP_077010.1:n.768+1_768+2delinsGT