Canonical Allele Identifier: CA801878187
Gene: SLC25A46 HGNC NCBI

Linked Data

dbSNP Id: rs1298587266
gnomAD v3: 5-110746186-A-G
gnomAD v4: 5-110746186-A-G
MyVariant Identifiers: chr5:g.110081887A>G (hg19) chr5:g.110746186A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110746186A>G , CM000667.2:g.110746186A>G GRCh38
NC_000005.9:g.110081887A>G , CM000667.1:g.110081887A>G GRCh37
NC_000005.8:g.110109786A>G NCBI36
NG_051334.1:g.13051A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355943.8:c.385-83A>G MANE Select ENSP00000348211.3:n.385-83A>G
ENST00000355943.7:c.385-83A>G ENSP00000348211.3:n.385-83A>G
ENST00000447245.6:c.385-83A>G ENSP00000399717.2:n.385-83A>G
ENST00000502462.6:n.618A>G
ENST00000504098.1:c.-54-83A>G ENSP00000425708.1:n.-54-83A>G
ENST00000508781.5:n.214-83A>G
ENST00000513807.5:c.-102-83A>G ENSP00000421134.1:n.-102-83A>G
NM_001303249.1:c.385-83A>G NP_001290178.1:n.385-83A>G
NM_001303250.1:c.112-83A>G NP_001290179.1:n.112-83A>G
NM_138773.2:c.385-83A>G NP_620128.1:n.385-83A>G
XM_011543708.1:c.385-83A>G XP_011542010.1:n.385-83A>G
NM_001303249.2:c.385-83A>G NP_001290178.1:n.385-83A>G
NM_001303250.2:c.112-83A>G NP_001290179.1:n.112-83A>G
NM_138773.3:c.385-83A>G NP_620128.1:n.385-83A>G
NR_138151.1:n.533-83A>G
NM_138773.4:c.385-83A>G MANE Select NP_620128.1:n.385-83A>G
NM_001303249.3:c.385-83A>G NP_001290178.1:n.385-83A>G
NM_001303250.3:c.112-83A>G NP_001290179.1:n.112-83A>G
NR_138151.2:n.498-83A>G
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