Canonical Allele Identifier: CA2657454075

Gene: ALG12

Linked Data

• gnomAD v4: 22-49913521-CGAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49913525_49913527del , CM000684.2:g.49913525_49913527del	GRCh38
NC_000022.10:g.50307173_50307175del , CM000684.1:g.50307173_50307175del	GRCh37
NC_000022.9:g.48693177_48693179del	NCBI36
NG_008927.1:g.9935_9937del

Transcript Alleles

HGVS	Amino-acid change
ENST00000330817.11:c.163-7_163-5del MANE Select	ENSP00000333813.5:n.163-7_163-5del
ENST00000330817.10:c.163-7_163-5del	ENSP00000333813.5:n.163-7_163-5del
NM_024105.3:c.163-7_163-5del	NP_077010.1:n.163-7_163-5del
XM_011530369.1:c.163-7_163-5del	XP_011528671.1:n.163-7_163-5del
XM_011530370.1:c.163-7_163-5del	XP_011528672.1:n.163-7_163-5del
XM_011530371.1:c.163-7_163-5del	XP_011528673.1:n.163-7_163-5del
XM_011530371.2:c.163-7_163-5del	XP_011528673.1:n.163-7_163-5del
XM_017028936.1:c.163-7_163-5del	XP_016884425.1:n.163-7_163-5del
XM_017028937.1:c.163-7_163-5del	XP_016884426.1:n.163-7_163-5del
NM_024105.4:c.163-7_163-5del MANE Select	NP_077010.1:n.163-7_163-5del