Canonical Allele Identifier: CA2410564848
Gene: ALG12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.49913626T= , CM000684.2:g.49913626T= GRCh38
NC_000022.10:g.50307274T= , CM000684.1:g.50307274T= GRCh37
NC_000022.9:g.48693278T= NCBI36
NG_008927.1:g.9833A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330817.11:c.140A= MANE Select ENSP00000333813.5:p.Tyr47=
ENST00000330817.10:c.140A= ENSP00000333813.5:p.Tyr47=
NM_024105.3:c.140A= NP_077010.1:p.Tyr47=
XM_011530369.1:c.140A= XP_011528671.1:p.Tyr47=
XM_011530370.1:c.140A= XP_011528672.1:p.Tyr47=
XM_011530371.1:c.140A= XP_011528673.1:p.Tyr47=
XM_011530371.2:c.140A= XP_011528673.1:p.Tyr47=
XM_017028936.1:c.140A= XP_016884425.1:p.Tyr47=
XM_017028937.1:c.140A= XP_016884426.1:p.Tyr47=
NM_024105.4:c.140A= MANE Select NP_077010.1:p.Tyr47=