Canonical Allele Identifier: CA2410564730
Gene: ALG12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.49913419C= , CM000684.2:g.49913419C= GRCh38
NC_000022.10:g.50307067C= , CM000684.1:g.50307067C= GRCh37
NC_000022.9:g.48693071C= NCBI36
NG_008927.1:g.10040G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330817.11:c.261G= MANE Select ENSP00000333813.5:p.Leu87=
ENST00000330817.10:c.261G= ENSP00000333813.5:p.Leu87=
NM_024105.3:c.261G= NP_077010.1:p.Leu87=
XM_011530369.1:c.261G= XP_011528671.1:p.Leu87=
XM_011530370.1:c.261G= XP_011528672.1:p.Leu87=
XM_011530371.1:c.261G= XP_011528673.1:p.Leu87=
XM_011530371.2:c.261G= XP_011528673.1:p.Leu87=
XM_017028936.1:c.261G= XP_016884425.1:p.Leu87=
XM_017028937.1:c.261G= XP_016884426.1:p.Leu87=
NM_024105.4:c.261G= MANE Select NP_077010.1:p.Leu87=