Canonical Allele Identifier: CA2740671417
Gene: SLC25A46 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110761199T>G , CM000667.2:g.110761199T>G GRCh38
NC_000005.9:g.110096899T>G , CM000667.1:g.110096899T>G GRCh37
NC_000005.8:g.110124798T>G NCBI36
NG_051334.1:g.28064T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355943.8:c.679-5T>G MANE Select ENSP00000348211.3:n.679-5T>G
ENST00000355943.7:c.679-5T>G ENSP00000348211.3:n.679-5T>G
ENST00000447245.6:c.679-248T>G ENSP00000399717.2:n.679-248T>G
ENST00000502462.6:n.995-5T>G
ENST00000504098.1:c.241-5T>G ENSP00000425708.1:n.241-5T>G
ENST00000509432.1:c.40-5T>G ENSP00000426604.1:n.40-5T>G
ENST00000513706.2:n.2279-5T>G
ENST00000513807.5:c.193-5T>G ENSP00000421134.1:n.193-5T>G
NM_001303249.1:c.679-248T>G NP_001290178.1:n.679-248T>G
NM_001303250.1:c.406-5T>G NP_001290179.1:n.406-5T>G
NM_138773.2:c.679-5T>G NP_620128.1:n.679-5T>G
NM_001303249.2:c.679-248T>G NP_001290178.1:n.679-248T>G
NM_001303250.2:c.406-5T>G NP_001290179.1:n.406-5T>G
NM_138773.3:c.679-5T>G NP_620128.1:n.679-5T>G
NR_138151.1:n.953-5T>G
NM_138773.4:c.679-5T>G MANE Select NP_620128.1:n.679-5T>G
NM_001303249.3:c.679-248T>G NP_001290178.1:n.679-248T>G
NM_001303250.3:c.406-5T>G NP_001290179.1:n.406-5T>G
NR_138151.2:n.918-5T>G