Canonical Allele Identifier: CA360697805
Gene: SLC25A46 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110761733T>A , CM000667.2:g.110761733T>A GRCh38
NC_000005.9:g.110097433T>A , CM000667.1:g.110097433T>A GRCh37
NC_000005.8:g.110125332T>A NCBI36
NG_051334.1:g.28598T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355943.8:c.1208T>A MANE Select ENSP00000348211.3:p.Leu403Ter
ENST00000355943.7:c.1208T>A ENSP00000348211.3:p.Leu403Ter
ENST00000447245.6:c.965T>A ENSP00000399717.2:p.Leu322Ter
ENST00000504098.1:c.770T>A ENSP00000425708.1:p.Leu257Ter
ENST00000509432.1:c.569T>A ENSP00000426604.1:p.Leu190Ter
ENST00000513706.2:n.2808T>A
ENST00000513807.5:c.722T>A ENSP00000421134.1:p.Leu241Ter
NM_001303249.1:c.965T>A NP_001290178.1:p.Leu322Ter
NM_001303250.1:c.935T>A NP_001290179.1:p.Leu312Ter
NM_138773.2:c.1208T>A NP_620128.1:p.Leu403Ter
NM_001303249.2:c.965T>A NP_001290178.1:p.Leu322Ter
NM_001303250.2:c.935T>A NP_001290179.1:p.Leu312Ter
NM_138773.3:c.1208T>A NP_620128.1:p.Leu403Ter
NR_138151.1:n.1482T>A
NM_138773.4:c.1208T>A MANE Select NP_620128.1:p.Leu403Ter
NM_001303249.3:c.965T>A NP_001290178.1:p.Leu322Ter
NM_001303250.3:c.935T>A NP_001290179.1:p.Leu312Ter
NR_138151.2:n.1447T>A