Canonical Allele Identifier: CA1572423639
Gene: SLC25A46 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110761451T= , CM000667.2:g.110761451T= GRCh38
NC_000005.9:g.110097151T= , CM000667.1:g.110097151T= GRCh37
NC_000005.8:g.110125050T= NCBI36
NG_051334.1:g.28316T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355943.8:c.926T= MANE Select ENSP00000348211.3:p.Met309=
ENST00000355943.7:c.926T= ENSP00000348211.3:p.Met309=
ENST00000447245.6:c.683T= ENSP00000399717.2:p.Met228=
ENST00000502462.6:n.1242T=
ENST00000504098.1:c.488T= ENSP00000425708.1:p.Met163=
ENST00000509432.1:c.287T= ENSP00000426604.1:p.Met96=
ENST00000513706.2:n.2526T=
ENST00000513807.5:c.440T= ENSP00000421134.1:p.Met147=
NM_001303249.1:c.683T= NP_001290178.1:p.Met228=
NM_001303250.1:c.653T= NP_001290179.1:p.Met218=
NM_138773.2:c.926T= NP_620128.1:p.Met309=
NM_001303249.2:c.683T= NP_001290178.1:p.Met228=
NM_001303250.2:c.653T= NP_001290179.1:p.Met218=
NM_138773.3:c.926T= NP_620128.1:p.Met309=
NR_138151.1:n.1200T=
NM_138773.4:c.926T= MANE Select NP_620128.1:p.Met309=
NM_001303249.3:c.683T= NP_001290178.1:p.Met228=
NM_001303250.3:c.653T= NP_001290179.1:p.Met218=
NR_138151.2:n.1165T=