Canonical Allele Identifier: CA2646117981
Gene: SLC35D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054085del , CM000663.2:g.67054085del GRCh38
NC_000001.10:g.67519768del , CM000663.1:g.67519768del GRCh37
NC_000001.9:g.67292356del NCBI36
NG_012933.1:g.5316del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-69del MANE Select ENSP00000235345.5:n.-69del
ENST00000235345.5:c.-69del ENSP00000235345.5:n.-69del
NM_015139.2:c.-69del NP_055954.1:n.-69del
XM_006710478.1:c.-69del XP_006710541.1:n.-69del
XM_011541070.1:c.-69del XP_011539372.1:n.-69del
XM_006710478.2:c.-69del XP_006710541.1:n.-69del
XM_011541070.2:c.-69del XP_011539372.1:n.-69del
XR_001737057.2:n.342del
XR_001737058.2:n.335del
NM_015139.3:c.-69del MANE Select NP_055954.1:n.-69del