Canonical Allele Identifier: CA360697789
Gene: SLC25A46 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110761727C>G , CM000667.2:g.110761727C>G GRCh38
NC_000005.9:g.110097427C>G , CM000667.1:g.110097427C>G GRCh37
NC_000005.8:g.110125326C>G NCBI36
NG_051334.1:g.28592C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355943.8:c.1202C>G MANE Select ENSP00000348211.3:p.Ala401Gly
ENST00000355943.7:c.1202C>G ENSP00000348211.3:p.Ala401Gly
ENST00000447245.6:c.959C>G ENSP00000399717.2:p.Ala320Gly
ENST00000504098.1:c.764C>G ENSP00000425708.1:p.Ala255Gly
ENST00000509432.1:c.563C>G ENSP00000426604.1:p.Ala188Gly
ENST00000513706.2:n.2802C>G
ENST00000513807.5:c.716C>G ENSP00000421134.1:p.Ala239Gly
NM_001303249.1:c.959C>G NP_001290178.1:p.Ala320Gly
NM_001303250.1:c.929C>G NP_001290179.1:p.Ala310Gly
NM_138773.2:c.1202C>G NP_620128.1:p.Ala401Gly
NM_001303249.2:c.959C>G NP_001290178.1:p.Ala320Gly
NM_001303250.2:c.929C>G NP_001290179.1:p.Ala310Gly
NM_138773.3:c.1202C>G NP_620128.1:p.Ala401Gly
NR_138151.1:n.1476C>G
NM_138773.4:c.1202C>G MANE Select NP_620128.1:p.Ala401Gly
NM_001303249.3:c.959C>G NP_001290178.1:p.Ala320Gly
NM_001303250.3:c.929C>G NP_001290179.1:p.Ala310Gly
NR_138151.2:n.1441C>G