Canonical Allele Identifier: CA445964699
Gene: SLC25A46 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110097452T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110761752T>A , CM000667.2:g.110761752T>A GRCh38
NC_000005.9:g.110097452T>A , CM000667.1:g.110097452T>A GRCh37
NC_000005.8:g.110125351T>A NCBI36
NG_051334.1:g.28617T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355943.8:c.1227T>A MANE Select ENSP00000348211.3:p.Ile409=
ENST00000355943.7:c.1227T>A ENSP00000348211.3:p.Ile409=
ENST00000447245.6:c.984T>A ENSP00000399717.2:p.Ile328=
ENST00000504098.1:c.789T>A ENSP00000425708.1:p.Ile263=
ENST00000509432.1:c.588T>A ENSP00000426604.1:p.Ile196=
ENST00000513706.2:n.2827T>A
ENST00000513807.5:c.741T>A ENSP00000421134.1:p.Ile247=
NM_001303249.1:c.984T>A NP_001290178.1:p.Ile328=
NM_001303250.1:c.954T>A NP_001290179.1:p.Ile318=
NM_138773.2:c.1227T>A NP_620128.1:p.Ile409=
NM_001303249.2:c.984T>A NP_001290178.1:p.Ile328=
NM_001303250.2:c.954T>A NP_001290179.1:p.Ile318=
NM_138773.3:c.1227T>A NP_620128.1:p.Ile409=
NR_138151.1:n.1501T>A
NM_138773.4:c.1227T>A MANE Select NP_620128.1:p.Ile409=
NM_001303249.3:c.984T>A NP_001290178.1:p.Ile328=
NM_001303250.3:c.954T>A NP_001290179.1:p.Ile318=
NR_138151.2:n.1466T>A