Canonical Allele Identifier: CA412081568
Gene: ALG12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.49913705C>G , CM000684.2:g.49913705C>G GRCh38
NC_000022.10:g.50307353C>G , CM000684.1:g.50307353C>G GRCh37
NC_000022.9:g.48693357C>G NCBI36
NG_008927.1:g.9754G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000330817.11:c.61G>C MANE Select ENSP00000333813.5:p.Ala21Pro
ENST00000330817.10:c.61G>C ENSP00000333813.5:p.Ala21Pro
NM_024105.3:c.61G>C NP_077010.1:p.Ala21Pro
XM_011530369.1:c.61G>C XP_011528671.1:p.Ala21Pro
XM_011530370.1:c.61G>C XP_011528672.1:p.Ala21Pro
XM_011530371.1:c.61G>C XP_011528673.1:p.Ala21Pro
XM_011530371.2:c.61G>C XP_011528673.1:p.Ala21Pro
XM_017028936.1:c.61G>C XP_016884425.1:p.Ala21Pro
XM_017028937.1:c.61G>C XP_016884426.1:p.Ala21Pro
NM_024105.4:c.61G>C MANE Select NP_077010.1:p.Ala21Pro