Canonical Allele Identifier: CA2646118000
Gene: SLC35D1 HGNC NCBI

Linked Data

gnomAD v4: 1-67054111-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054111T>C , CM000663.2:g.67054111T>C GRCh38
NC_000001.10:g.67519794T>C , CM000663.1:g.67519794T>C GRCh37
NC_000001.9:g.67292382T>C NCBI36
NG_012933.1:g.5287A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-98A>G MANE Select ENSP00000235345.5:n.-98A>G
NM_015139.2:c.-98A>G NP_055954.1:n.-98A>G
XM_006710478.1:c.-98A>G XP_006710541.1:n.-98A>G
XM_011541070.1:c.-98A>G XP_011539372.1:n.-98A>G
XM_006710478.2:c.-98A>G XP_006710541.1:n.-98A>G
XM_011541070.2:c.-98A>G XP_011539372.1:n.-98A>G
XR_001737057.2:n.313A>G
XR_001737058.2:n.306A>G
NM_015139.3:c.-98A>G MANE Select NP_055954.1:n.-98A>G
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