Canonical Allele Identifier: CA2674823544
Gene: SLC25A46 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110761072_110761073insCTA , CM000667.2:g.110761072_110761073insCTA GRCh38
NC_000005.9:g.110096772_110096773insCTA , CM000667.1:g.110096772_110096773insCTA GRCh37
NC_000005.8:g.110124671_110124672insCTA NCBI36
NG_051334.1:g.27937_27938insCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355943.8:c.679-132_679-131insCTA MANE Select ENSP00000348211.3:n.679-132_679-131insCTA
ENST00000355943.7:c.679-132_679-131insCTA ENSP00000348211.3:n.679-132_679-131insCTA
ENST00000447245.6:c.679-375_679-374insCTA ENSP00000399717.2:n.679-375_679-374insCTA
ENST00000502462.6:n.995-132_995-131insCTA
ENST00000504098.1:c.241-132_241-131insCTA ENSP00000425708.1:n.241-132_241-131insCTA
ENST00000509432.1:c.40-132_40-131insCTA ENSP00000426604.1:n.40-132_40-131insCTA
ENST00000513706.2:n.2279-132_2279-131insCTA
ENST00000513807.5:c.193-132_193-131insCTA ENSP00000421134.1:n.193-132_193-131insCTA
NM_001303249.1:c.679-375_679-374insCTA NP_001290178.1:n.679-375_679-374insCTA
NM_001303250.1:c.406-132_406-131insCTA NP_001290179.1:n.406-132_406-131insCTA
NM_138773.2:c.679-132_679-131insCTA NP_620128.1:n.679-132_679-131insCTA
NM_001303249.2:c.679-375_679-374insCTA NP_001290178.1:n.679-375_679-374insCTA
NM_001303250.2:c.406-132_406-131insCTA NP_001290179.1:n.406-132_406-131insCTA
NM_138773.3:c.679-132_679-131insCTA NP_620128.1:n.679-132_679-131insCTA
NR_138151.1:n.953-132_953-131insCTA
NM_138773.4:c.679-132_679-131insCTA MANE Select NP_620128.1:n.679-132_679-131insCTA
NM_001303249.3:c.679-375_679-374insCTA NP_001290178.1:n.679-375_679-374insCTA
NM_001303250.3:c.406-132_406-131insCTA NP_001290179.1:n.406-132_406-131insCTA
NR_138151.2:n.918-132_918-131insCTA