Canonical Allele Identifier: CA1572424030
Gene: SLC25A46 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110761703T= , CM000667.2:g.110761703T= GRCh38
NC_000005.9:g.110097403T= , CM000667.1:g.110097403T= GRCh37
NC_000005.8:g.110125302T= NCBI36
NG_051334.1:g.28568T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355943.8:c.1178T= MANE Select ENSP00000348211.3:p.Ile393=
ENST00000355943.7:c.1178T= ENSP00000348211.3:p.Ile393=
ENST00000447245.6:c.935T= ENSP00000399717.2:p.Ile312=
ENST00000504098.1:c.740T= ENSP00000425708.1:p.Ile247=
ENST00000509432.1:c.539T= ENSP00000426604.1:p.Ile180=
ENST00000513706.2:n.2778T=
ENST00000513807.5:c.692T= ENSP00000421134.1:p.Ile231=
NM_001303249.1:c.935T= NP_001290178.1:p.Ile312=
NM_001303250.1:c.905T= NP_001290179.1:p.Ile302=
NM_138773.2:c.1178T= NP_620128.1:p.Ile393=
NM_001303249.2:c.935T= NP_001290178.1:p.Ile312=
NM_001303250.2:c.905T= NP_001290179.1:p.Ile302=
NM_138773.3:c.1178T= NP_620128.1:p.Ile393=
NR_138151.1:n.1452T=
NM_138773.4:c.1178T= MANE Select NP_620128.1:p.Ile393=
NM_001303249.3:c.935T= NP_001290178.1:p.Ile312=
NM_001303250.3:c.905T= NP_001290179.1:p.Ile302=
NR_138151.2:n.1417T=