Canonical Allele Identifier: CA412081111

Gene: ALG12

Linked Data

• ClinVar Variation Id: 3061429
• ClinVar RCV Id: RCV003983437
• gnomAD v4: 22-49913658-G-C
• MyVariant Identifiers: chr22:g.50307306G>C (hg19) ; chr22:g.49913658G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49913658G>C , CM000684.2:g.49913658G>C	GRCh38
NC_000022.10:g.50307306G>C , CM000684.1:g.50307306G>C	GRCh37
NC_000022.9:g.48693310G>C	NCBI36
NG_008927.1:g.9801C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.108C>G MANE Select	ENSP00000333813.5:p.Ser36Arg
ENST00000330817.10:c.108C>G	ENSP00000333813.5:p.Ser36Arg
NM_024105.3:c.108C>G	NP_077010.1:p.Ser36Arg
XM_011530369.1:c.108C>G	XP_011528671.1:p.Ser36Arg
XM_011530370.1:c.108C>G	XP_011528672.1:p.Ser36Arg
XM_011530371.1:c.108C>G	XP_011528673.1:p.Ser36Arg
XM_011530371.2:c.108C>G	XP_011528673.1:p.Ser36Arg
XM_017028936.1:c.108C>G	XP_016884425.1:p.Ser36Arg
XM_017028937.1:c.108C>G	XP_016884426.1:p.Ser36Arg
NM_024105.4:c.108C>G MANE Select	NP_077010.1:p.Ser36Arg