Canonical Allele Identifier: CA2410564938

Gene: ALG12

Linked Data

• dbSNP Id: rs2060595308
• gnomAD v4: 22-49913805-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49913805T>G , CM000684.2:g.49913805T>G	GRCh38
NC_000022.10:g.50307453T>G , CM000684.1:g.50307453T>G	GRCh37
NC_000022.9:g.48693457T>G	NCBI36
NG_008927.1:g.9654A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.-40A>C MANE Select	ENSP00000333813.5:n.-40A>C
ENST00000330817.10:c.-40A>C	ENSP00000333813.5:n.-40A>C
NM_024105.3:c.-40A>C	NP_077010.1:n.-40A>C
XM_011530369.1:c.-40A>C	XP_011528671.1:n.-40A>C
XM_011530370.1:c.-40A>C	XP_011528672.1:n.-40A>C
XM_011530371.1:c.-40A>C	XP_011528673.1:n.-40A>C
XM_011530371.2:c.-40A>C	XP_011528673.1:n.-40A>C
XM_017028936.1:c.-40A>C	XP_016884425.1:n.-40A>C
XM_017028937.1:c.-40A>C	XP_016884426.1:n.-40A>C
NM_024105.4:c.-40A>C MANE Select	NP_077010.1:n.-40A>C