Canonical Allele Identifier: CA1172975948
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs1645346480
gnomAD v4: 1-67054067-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054067C>T , CM000663.2:g.67054067C>T GRCh38
NC_000001.10:g.67519750C>T , CM000663.1:g.67519750C>T GRCh37
NC_000001.9:g.67292338C>T NCBI36
NG_012933.1:g.5331G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-54G>A MANE Select ENSP00000235345.5:n.-54G>A
ENST00000235345.5:c.-54G>A ENSP00000235345.5:n.-54G>A
NM_015139.2:c.-54G>A NP_055954.1:n.-54G>A
XM_006710478.1:c.-54G>A XP_006710541.1:n.-54G>A
XM_011541070.1:c.-54G>A XP_011539372.1:n.-54G>A
XM_006710478.2:c.-54G>A XP_006710541.1:n.-54G>A
XM_011541070.2:c.-54G>A XP_011539372.1:n.-54G>A
XR_001737057.2:n.357G>A
XR_001737058.2:n.350G>A
NM_015139.3:c.-54G>A MANE Select NP_055954.1:n.-54G>A
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