Canonical Allele Identifier: CA1172975915
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs1645346024

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054056_67054073del , CM000663.2:g.67054056_67054073del GRCh38
NC_000001.10:g.67519739_67519756del , CM000663.1:g.67519739_67519756del GRCh37
NC_000001.9:g.67292327_67292344del NCBI36
NG_012933.1:g.5331_5348del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-54_-37del MANE Select ENSP00000235345.5:n.-54_-37del
ENST00000235345.5:c.-54_-37del ENSP00000235345.5:n.-54_-37del
NM_015139.2:c.-54_-37del NP_055954.1:n.-54_-37del
XM_006710478.1:c.-54_-37del XP_006710541.1:n.-54_-37del
XM_011541070.1:c.-54_-37del XP_011539372.1:n.-54_-37del
XM_006710478.2:c.-54_-37del XP_006710541.1:n.-54_-37del
XM_011541070.2:c.-54_-37del XP_011539372.1:n.-54_-37del
XR_001737057.2:n.357_374del
XR_001737058.2:n.350_367del
NM_015139.3:c.-54_-37del MANE Select NP_055954.1:n.-54_-37del