Canonical Allele Identifier: CA360694338
Gene: SLC25A46 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110081969G>C (hg19) chr5:g.110746268G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110746268G>C , CM000667.2:g.110746268G>C GRCh38
NC_000005.9:g.110081969G>C , CM000667.1:g.110081969G>C GRCh37
NC_000005.8:g.110109868G>C NCBI36
NG_051334.1:g.13133G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000355943.8:c.385-1G>C MANE Select ENSP00000348211.3:n.385-1G>C
ENST00000355943.7:c.385-1G>C ENSP00000348211.3:n.385-1G>C
ENST00000447245.6:c.385-1G>C ENSP00000399717.2:n.385-1G>C
ENST00000502462.6:n.700G>C
ENST00000504098.1:c.-54-1G>C ENSP00000425708.1:n.-54-1G>C
ENST00000508781.5:n.214-1G>C
ENST00000513807.5:c.-102-1G>C ENSP00000421134.1:n.-102-1G>C
NM_001303249.1:c.385-1G>C NP_001290178.1:n.385-1G>C
NM_001303250.1:c.112-1G>C NP_001290179.1:n.112-1G>C
NM_138773.2:c.385-1G>C NP_620128.1:n.385-1G>C
XM_011543708.1:c.385-1G>C XP_011542010.1:n.385-1G>C
NM_001303249.2:c.385-1G>C NP_001290178.1:n.385-1G>C
NM_001303250.2:c.112-1G>C NP_001290179.1:n.112-1G>C
NM_138773.3:c.385-1G>C NP_620128.1:n.385-1G>C
NR_138151.1:n.533-1G>C
NM_138773.4:c.385-1G>C MANE Select NP_620128.1:n.385-1G>C
NM_001303249.3:c.385-1G>C NP_001290178.1:n.385-1G>C
NM_001303250.3:c.112-1G>C NP_001290179.1:n.112-1G>C
NR_138151.2:n.498-1G>C
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