Canonical Allele Identifier: CA2646117986
Gene: SLC35D1 HGNC NCBI

Linked Data

gnomAD v4: 1-67054088-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054090del , CM000663.2:g.67054090del GRCh38
NC_000001.10:g.67519773del , CM000663.1:g.67519773del GRCh37
NC_000001.9:g.67292361del NCBI36
NG_012933.1:g.5309del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-76del MANE Select ENSP00000235345.5:n.-76del
ENST00000235345.5:c.-76del ENSP00000235345.5:n.-76del
NM_015139.2:c.-76del NP_055954.1:n.-76del
XM_006710478.1:c.-76del XP_006710541.1:n.-76del
XM_011541070.1:c.-76del XP_011539372.1:n.-76del
XM_006710478.2:c.-76del XP_006710541.1:n.-76del
XM_011541070.2:c.-76del XP_011539372.1:n.-76del
XR_001737057.2:n.335del
XR_001737058.2:n.328del
NM_015139.3:c.-76del MANE Select NP_055954.1:n.-76del
Search 100 bp 5'
Search 100 bp 3'