Canonical Allele Identifier: CA418233664
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67021724_67021731del , CM000663.2:g.67021724_67021731del GRCh38
NC_000001.10:g.67487407_67487414del , CM000663.1:g.67487407_67487414del GRCh37
NC_000001.9:g.67259995_67260002del NCBI36
NG_012933.1:g.37672_37679del

Transcript Alleles

HGVS Amino-acid Change
NM_015139.3:c.730-124_730-117del MANE Select NP_055954.1:n.730-124_730-117del
ENST00000235345.6:c.730-124_730-117del MANE Select ENSP00000235345.5:n.730-124_730-117del
NM_015139.2:c.730-124_730-117del NP_055954.1:n.730-124_730-117del
ENST00000235345.5:c.730-124_730-117del ENSP00000235345.5:n.730-124_730-117del
XM_006710478.1:c.811-124_811-117del XP_006710541.1:n.811-124_811-117del
XM_006710478.2:c.811-124_811-117del XP_006710541.1:n.811-124_811-117del
XM_011541070.1:c.811-124_811-117del XP_011539372.1:n.811-124_811-117del
XM_011541070.2:c.811-124_811-117del XP_011539372.1:n.811-124_811-117del
XR_001737057.2:n.1221-124_1221-117del
XR_001737058.2:n.1133-124_1133-117del