Canonical Allele Identifier: CA2410564778
Gene: ALG12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.49913514C= , CM000684.2:g.49913514C= GRCh38
NC_000022.10:g.50307162C= , CM000684.1:g.50307162C= GRCh37
NC_000022.9:g.48693166C= NCBI36
NG_008927.1:g.9945G=

Transcript Alleles

HGVS Amino-acid change
ENST00000330817.11:c.166G= MANE Select ENSP00000333813.5:p.Asp56=
ENST00000330817.10:c.166G= ENSP00000333813.5:p.Asp56=
NM_024105.3:c.166G= NP_077010.1:p.Asp56=
XM_011530369.1:c.166G= XP_011528671.1:p.Asp56=
XM_011530370.1:c.166G= XP_011528672.1:p.Asp56=
XM_011530371.1:c.166G= XP_011528673.1:p.Asp56=
XM_011530371.2:c.166G= XP_011528673.1:p.Asp56=
XM_017028936.1:c.166G= XP_016884425.1:p.Asp56=
XM_017028937.1:c.166G= XP_016884426.1:p.Asp56=
NM_024105.4:c.166G= MANE Select NP_077010.1:p.Asp56=