Canonical Allele Identifier: CA360696137
Gene: SLC25A46 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110761282C>G , CM000667.2:g.110761282C>G GRCh38
NC_000005.9:g.110096982C>G , CM000667.1:g.110096982C>G GRCh37
NC_000005.8:g.110124881C>G NCBI36
NG_051334.1:g.28147C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355943.8:c.757C>G MANE Select ENSP00000348211.3:p.Pro253Ala
ENST00000355943.7:c.757C>G ENSP00000348211.3:p.Pro253Ala
ENST00000447245.6:c.679-165C>G ENSP00000399717.2:n.679-165C>G
ENST00000502462.6:n.1073C>G
ENST00000504098.1:c.319C>G ENSP00000425708.1:p.Pro107Ala
ENST00000509432.1:c.118C>G ENSP00000426604.1:p.Pro40Ala
ENST00000513706.2:n.2357C>G
ENST00000513807.5:c.271C>G ENSP00000421134.1:p.Pro91Ala
NM_001303249.1:c.679-165C>G NP_001290178.1:n.679-165C>G
NM_001303250.1:c.484C>G NP_001290179.1:p.Pro162Ala
NM_138773.2:c.757C>G NP_620128.1:p.Pro253Ala
NM_001303249.2:c.679-165C>G NP_001290178.1:n.679-165C>G
NM_001303250.2:c.484C>G NP_001290179.1:p.Pro162Ala
NM_138773.3:c.757C>G NP_620128.1:p.Pro253Ala
NR_138151.1:n.1031C>G
NM_138773.4:c.757C>G MANE Select NP_620128.1:p.Pro253Ala
NM_001303249.3:c.679-165C>G NP_001290178.1:n.679-165C>G
NM_001303250.3:c.484C>G NP_001290179.1:p.Pro162Ala
NR_138151.2:n.996C>G