Canonical Allele Identifier: CA2574400878
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054033del , CM000663.2:g.67054033del GRCh38
NC_000001.10:g.67519716del , CM000663.1:g.67519716del GRCh37
NC_000001.9:g.67292304del NCBI36
NG_012933.1:g.5366del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-19del MANE Select ENSP00000235345.5:n.-19del
ENST00000235345.5:c.-19del ENSP00000235345.5:n.-19del
NM_015139.2:c.-19del NP_055954.1:n.-19del
XM_006710478.1:c.-19del XP_006710541.1:n.-19del
XM_011541070.1:c.-19del XP_011539372.1:n.-19del
XM_006710478.2:c.-19del XP_006710541.1:n.-19del
XM_011541070.2:c.-19del XP_011539372.1:n.-19del
XR_001737057.2:n.392del
XR_001737058.2:n.385del
NM_015139.3:c.-19del MANE Select NP_055954.1:n.-19del