Canonical Allele Identifier: CA412080055
Gene: ALG12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.49913484T>C , CM000684.2:g.49913484T>C GRCh38
NC_000022.10:g.50307132T>C , CM000684.1:g.50307132T>C GRCh37
NC_000022.9:g.48693136T>C NCBI36
NG_008927.1:g.9975A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000330817.11:c.196A>G MANE Select ENSP00000333813.5:p.Arg66Gly
ENST00000330817.10:c.196A>G ENSP00000333813.5:p.Arg66Gly
NM_024105.3:c.196A>G NP_077010.1:p.Arg66Gly
XM_011530369.1:c.196A>G XP_011528671.1:p.Arg66Gly
XM_011530370.1:c.196A>G XP_011528672.1:p.Arg66Gly
XM_011530371.1:c.196A>G XP_011528673.1:p.Arg66Gly
XM_011530371.2:c.196A>G XP_011528673.1:p.Arg66Gly
XM_017028936.1:c.196A>G XP_016884425.1:p.Arg66Gly
XM_017028937.1:c.196A>G XP_016884426.1:p.Arg66Gly
NM_024105.4:c.196A>G MANE Select NP_077010.1:p.Arg66Gly