Canonical Allele Identifier: CA2657449386

Gene: ALG12

Linked Data

• gnomAD v4: 22-49913909-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49913909G>T , CM000684.2:g.49913909G>T	GRCh38
NC_000022.10:g.50307557G>T , CM000684.1:g.50307557G>T	GRCh37
NC_000022.9:g.48693561G>T	NCBI36
NG_008927.1:g.9550C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.-78-66C>A MANE Select	ENSP00000333813.5:n.-78-66C>A
ENST00000330817.10:c.-78-66C>A	ENSP00000333813.5:n.-78-66C>A
NM_024105.3:c.-78-66C>A	NP_077010.1:n.-78-66C>A
XM_011530369.1:c.-78-66C>A	XP_011528671.1:n.-78-66C>A
XM_011530370.1:c.-78-66C>A	XP_011528672.1:n.-78-66C>A
XM_011530371.1:c.-78-66C>A	XP_011528673.1:n.-78-66C>A
XM_011530371.2:c.-78-66C>A	XP_011528673.1:n.-78-66C>A
XM_017028936.1:c.-78-66C>A	XP_016884425.1:n.-78-66C>A
XM_017028937.1:c.-78-66C>A	XP_016884426.1:n.-78-66C>A
NM_024105.4:c.-78-66C>A MANE Select	NP_077010.1:n.-78-66C>A