Canonical Allele Identifier: CA2657449435

Gene: ALG12

Linked Data

• gnomAD v4: 22-49913966-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49913966T>C , CM000684.2:g.49913966T>C	GRCh38
NC_000022.10:g.50307614T>C , CM000684.1:g.50307614T>C	GRCh37
NC_000022.9:g.48693618T>C	NCBI36
NG_008927.1:g.9493A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.-78-123A>G MANE Select	ENSP00000333813.5:n.-78-123A>G
ENST00000330817.10:c.-78-123A>G	ENSP00000333813.5:n.-78-123A>G
NM_024105.3:c.-78-123A>G	NP_077010.1:n.-78-123A>G
XM_011530369.1:c.-78-123A>G	XP_011528671.1:n.-78-123A>G
XM_011530370.1:c.-78-123A>G	XP_011528672.1:n.-78-123A>G
XM_011530371.1:c.-78-123A>G	XP_011528673.1:n.-78-123A>G
XM_011530371.2:c.-78-123A>G	XP_011528673.1:n.-78-123A>G
XM_017028936.1:c.-78-123A>G	XP_016884425.1:n.-78-123A>G
XM_017028937.1:c.-78-123A>G	XP_016884426.1:n.-78-123A>G
NM_024105.4:c.-78-123A>G MANE Select	NP_077010.1:n.-78-123A>G