Canonical Allele Identifier: CA1572424099
Gene: SLC25A46 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110761747_110761751delinsATTAT , CM000667.2:g.110761747_110761751delinsATTAT GRCh38
NC_000005.9:g.110097447_110097451delinsATTAT , CM000667.1:g.110097447_110097451delinsATTAT GRCh37
NC_000005.8:g.110125346_110125350delinsATTAT NCBI36
NG_051334.1:g.28612_28616delinsATTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355943.8:c.1222_1226delinsATTAT MANE Select ENSP00000348211.3:p.Ile408=
ENST00000355943.7:c.1222_1226delinsATTAT ENSP00000348211.3:p.Ile408=
ENST00000447245.6:c.979_983delinsATTAT ENSP00000399717.2:p.Ile327=
ENST00000504098.1:c.784_788delinsATTAT ENSP00000425708.1:p.Ile262=
ENST00000509432.1:c.583_587delinsATTAT ENSP00000426604.1:p.Ile195=
ENST00000513706.2:n.2822_2826delinsATTAT
ENST00000513807.5:c.736_740delinsATTAT ENSP00000421134.1:p.Ile246=
NM_001303249.1:c.979_983delinsATTAT NP_001290178.1:p.Ile327=
NM_001303250.1:c.949_953delinsATTAT NP_001290179.1:p.Ile317=
NM_138773.2:c.1222_1226delinsATTAT NP_620128.1:p.Ile408=
NM_001303249.2:c.979_983delinsATTAT NP_001290178.1:p.Ile327=
NM_001303250.2:c.949_953delinsATTAT NP_001290179.1:p.Ile317=
NM_138773.3:c.1222_1226delinsATTAT NP_620128.1:p.Ile408=
NR_138151.1:n.1496_1500delinsATTAT
NM_138773.4:c.1222_1226delinsATTAT MANE Select NP_620128.1:p.Ile408=
NM_001303249.3:c.979_983delinsATTAT NP_001290178.1:p.Ile327=
NM_001303250.3:c.949_953delinsATTAT NP_001290179.1:p.Ile317=
NR_138151.2:n.1461_1465delinsATTAT