Canonical Allele Identifier: CA2674821570
Gene: SLC25A46 HGNC NCBI

Linked Data

gnomAD v4: 5-110746183-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110746183T>C , CM000667.2:g.110746183T>C GRCh38
NC_000005.9:g.110081884T>C , CM000667.1:g.110081884T>C GRCh37
NC_000005.8:g.110109783T>C NCBI36
NG_051334.1:g.13048T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000355943.8:c.385-86T>C MANE Select ENSP00000348211.3:n.385-86T>C
ENST00000355943.7:c.385-86T>C ENSP00000348211.3:n.385-86T>C
ENST00000447245.6:c.385-86T>C ENSP00000399717.2:n.385-86T>C
ENST00000502462.6:n.615T>C
ENST00000504098.1:c.-54-86T>C ENSP00000425708.1:n.-54-86T>C
ENST00000508781.5:n.214-86T>C
ENST00000513807.5:c.-102-86T>C ENSP00000421134.1:n.-102-86T>C
NM_001303249.1:c.385-86T>C NP_001290178.1:n.385-86T>C
NM_001303250.1:c.112-86T>C NP_001290179.1:n.112-86T>C
NM_138773.2:c.385-86T>C NP_620128.1:n.385-86T>C
XM_011543708.1:c.385-86T>C XP_011542010.1:n.385-86T>C
NM_001303249.2:c.385-86T>C NP_001290178.1:n.385-86T>C
NM_001303250.2:c.112-86T>C NP_001290179.1:n.112-86T>C
NM_138773.3:c.385-86T>C NP_620128.1:n.385-86T>C
NR_138151.1:n.533-86T>C
NM_138773.4:c.385-86T>C MANE Select NP_620128.1:n.385-86T>C
NM_001303249.3:c.385-86T>C NP_001290178.1:n.385-86T>C
NM_001303250.3:c.112-86T>C NP_001290179.1:n.112-86T>C
NR_138151.2:n.498-86T>C
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