Canonical Allele Identifier: CA1572423061
Gene: SLC25A46 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110761091G= , CM000667.2:g.110761091G= GRCh38
NC_000005.9:g.110096791G= , CM000667.1:g.110096791G= GRCh37
NC_000005.8:g.110124690G= NCBI36
NG_051334.1:g.27956G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355943.8:c.679-113G= MANE Select ENSP00000348211.3:n.679-113G=
ENST00000355943.7:c.679-113G= ENSP00000348211.3:n.679-113G=
ENST00000447245.6:c.679-356G= ENSP00000399717.2:n.679-356G=
ENST00000502462.6:n.995-113G=
ENST00000504098.1:c.241-113G= ENSP00000425708.1:n.241-113G=
ENST00000509432.1:c.40-113G= ENSP00000426604.1:n.40-113G=
ENST00000513706.2:n.2279-113G=
ENST00000513807.5:c.193-113G= ENSP00000421134.1:n.193-113G=
NM_001303249.1:c.679-356G= NP_001290178.1:n.679-356G=
NM_001303250.1:c.406-113G= NP_001290179.1:n.406-113G=
NM_138773.2:c.679-113G= NP_620128.1:n.679-113G=
NM_001303249.2:c.679-356G= NP_001290178.1:n.679-356G=
NM_001303250.2:c.406-113G= NP_001290179.1:n.406-113G=
NM_138773.3:c.679-113G= NP_620128.1:n.679-113G=
NR_138151.1:n.953-113G=
NM_138773.4:c.679-113G= MANE Select NP_620128.1:n.679-113G=
NM_001303249.3:c.679-356G= NP_001290178.1:n.679-356G=
NM_001303250.3:c.406-113G= NP_001290179.1:n.406-113G=
NR_138151.2:n.918-113G=