Canonical Allele Identifier: CA2646116169
Gene: SLC35D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009320_67009323del , CM000663.2:g.67009320_67009323del GRCh38
NC_000001.10:g.67475003_67475006del , CM000663.1:g.67475003_67475006del GRCh37
NC_000001.9:g.67247591_67247594del NCBI36
NG_012933.1:g.50078_50081del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.877-153_877-150del MANE Select ENSP00000235345.5:n.877-153_877-150del
ENST00000235345.5:c.877-153_877-150del ENSP00000235345.5:n.877-153_877-150del
NM_015139.2:c.877-153_877-150del NP_055954.1:n.877-153_877-150del
XM_006710478.1:c.958-153_958-150del XP_006710541.1:n.958-153_958-150del
XM_011541070.1:c.958-153_958-150del XP_011539372.1:n.958-153_958-150del
XM_006710478.2:c.958-153_958-150del XP_006710541.1:n.958-153_958-150del
XM_011541070.2:c.958-153_958-150del XP_011539372.1:n.958-153_958-150del
XR_001737057.2:n.1461-153_1461-150del
XR_001737058.2:n.2246-153_2246-150del
NM_015139.3:c.877-153_877-150del MANE Select NP_055954.1:n.877-153_877-150del