Canonical Allele Identifier: CA2657455164

Gene: ALG12

Linked Data

• gnomAD v4: 22-49913859-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49913861_49913862del , CM000684.2:g.49913861_49913862del	GRCh38
NC_000022.10:g.50307509_50307510del , CM000684.1:g.50307509_50307510del	GRCh37
NC_000022.9:g.48693513_48693514del	NCBI36
NG_008927.1:g.9598_9599del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.-78-18_-78-17del MANE Select	ENSP00000333813.5:n.-78-18_-78-17del
ENST00000330817.10:c.-78-18_-78-17del	ENSP00000333813.5:n.-78-18_-78-17del
NM_024105.3:c.-78-18_-78-17del	NP_077010.1:n.-78-18_-78-17del
XM_011530369.1:c.-78-18_-78-17del	XP_011528671.1:n.-78-18_-78-17del
XM_011530370.1:c.-78-18_-78-17del	XP_011528672.1:n.-78-18_-78-17del
XM_011530371.1:c.-78-18_-78-17del	XP_011528673.1:n.-78-18_-78-17del
XM_011530371.2:c.-78-18_-78-17del	XP_011528673.1:n.-78-18_-78-17del
XM_017028936.1:c.-78-18_-78-17del	XP_016884425.1:n.-78-18_-78-17del
XM_017028937.1:c.-78-18_-78-17del	XP_016884426.1:n.-78-18_-78-17del
NM_024105.4:c.-78-18_-78-17del MANE Select	NP_077010.1:n.-78-18_-78-17del