Canonical Allele Identifier: CA360696504

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097157A>T (hg19) ; chr5:g.110761457A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761457A>T , CM000667.2:g.110761457A>T	GRCh38
NC_000005.9:g.110097157A>T , CM000667.1:g.110097157A>T	GRCh37
NC_000005.8:g.110125056A>T	NCBI36
NG_051334.1:g.28322A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355943.8:c.932A>T MANE Select	ENSP00000348211.3:p.Asp311Val
ENST00000355943.7:c.932A>T	ENSP00000348211.3:p.Asp311Val
ENST00000447245.6:c.689A>T	ENSP00000399717.2:p.Asp230Val
ENST00000502462.6:n.1248A>T
ENST00000504098.1:c.494A>T	ENSP00000425708.1:p.Asp165Val
ENST00000509432.1:c.293A>T	ENSP00000426604.1:p.Asp98Val
ENST00000513706.2:n.2532A>T
ENST00000513807.5:c.446A>T	ENSP00000421134.1:p.Asp149Val
NM_001303249.1:c.689A>T	NP_001290178.1:p.Asp230Val
NM_001303250.1:c.659A>T	NP_001290179.1:p.Asp220Val
NM_138773.2:c.932A>T	NP_620128.1:p.Asp311Val
NM_001303249.2:c.689A>T	NP_001290178.1:p.Asp230Val
NM_001303250.2:c.659A>T	NP_001290179.1:p.Asp220Val
NM_138773.3:c.932A>T	NP_620128.1:p.Asp311Val
NR_138151.1:n.1206A>T
NM_138773.4:c.932A>T MANE Select	NP_620128.1:p.Asp311Val
NM_001303249.3:c.689A>T	NP_001290178.1:p.Asp230Val
NM_001303250.3:c.659A>T	NP_001290179.1:p.Asp220Val
NR_138151.2:n.1171A>T