Canonical Allele Identifier: CA1148088965
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053999A= , CM000663.2:g.67053999A= GRCh38
NC_000001.10:g.67519682A= , CM000663.1:g.67519682A= GRCh37
NC_000001.9:g.67292270A= NCBI36
NG_012933.1:g.5399T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.15T= MANE Select ENSP00000235345.5:p.His5=
ENST00000235345.5:c.15T= ENSP00000235345.5:p.His5=
NM_015139.2:c.15T= NP_055954.1:p.His5=
XM_006710478.1:c.15T= XP_006710541.1:p.His5=
XM_011541070.1:c.15T= XP_011539372.1:p.His5=
XM_006710478.2:c.15T= XP_006710541.1:p.His5=
XM_011541070.2:c.15T= XP_011539372.1:p.His5=
XR_001737057.2:n.425T=
XR_001737058.2:n.418T=
NM_015139.3:c.15T= MANE Select NP_055954.1:p.His5=