Canonical Allele Identifier: CA899210
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs752986033
ExAC: 1:67519713 G / GC
gnomAD v2: 1-67519713-G-GC
gnomAD v4: 1-67054030-G-GC
MyVariant Identifiers: chr1:g.67519713_67519714insC (hg19) chr1:g.67054030_67054031insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054030_67054031insC , CM000663.2:g.67054030_67054031insC GRCh38
NC_000001.10:g.67519713_67519714insC , CM000663.1:g.67519713_67519714insC GRCh37
NC_000001.9:g.67292301_67292302insC NCBI36
NG_012933.1:g.5367_5368insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-18_-17insG MANE Select ENSP00000235345.5:n.-18_-17insG
ENST00000235345.5:c.-18_-17insG ENSP00000235345.5:n.-18_-17insG
NM_015139.2:c.-18_-17insG NP_055954.1:n.-18_-17insG
XM_006710478.1:c.-18_-17insG XP_006710541.1:n.-18_-17insG
XM_011541070.1:c.-18_-17insG XP_011539372.1:n.-18_-17insG
XM_006710478.2:c.-18_-17insG XP_006710541.1:n.-18_-17insG
XM_011541070.2:c.-18_-17insG XP_011539372.1:n.-18_-17insG
XR_001737057.2:n.393_394insG
XR_001737058.2:n.386_387insG
NM_015139.3:c.-18_-17insG MANE Select NP_055954.1:n.-18_-17insG
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