Canonical Allele Identifier: CA360697995

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097480T>A (hg19) ; chr5:g.110761780T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761780T>A , CM000667.2:g.110761780T>A	GRCh38
NC_000005.9:g.110097480T>A , CM000667.1:g.110097480T>A	GRCh37
NC_000005.8:g.110125379T>A	NCBI36
NG_051334.1:g.28645T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1255T>A MANE Select	ENSP00000348211.3:p.Ter419Arg
ENST00000355943.7:c.1255T>A	ENSP00000348211.3:p.Ter419Arg
ENST00000447245.6:c.1012T>A	ENSP00000399717.2:p.Ter338Arg
ENST00000504098.1:c.817T>A	ENSP00000425708.1:p.Ter273Arg
ENST00000509432.1:c.616T>A	ENSP00000426604.1:p.Ter206Arg
ENST00000513706.2:n.2855T>A
ENST00000513807.5:c.769T>A	ENSP00000421134.1:p.Ter257Arg
NM_001303249.1:c.1012T>A	NP_001290178.1:p.Ter338Arg
NM_001303250.1:c.982T>A	NP_001290179.1:p.Ter328Arg
NM_138773.2:c.1255T>A	NP_620128.1:p.Ter419Arg
NM_001303249.2:c.1012T>A	NP_001290178.1:p.Ter338Arg
NM_001303250.2:c.982T>A	NP_001290179.1:p.Ter328Arg
NM_138773.3:c.1255T>A	NP_620128.1:p.Ter419Arg
NR_138151.1:n.1529T>A
NM_138773.4:c.1255T>A MANE Select	NP_620128.1:p.Ter419Arg
NM_001303249.3:c.1012T>A	NP_001290178.1:p.Ter338Arg
NM_001303250.3:c.982T>A	NP_001290179.1:p.Ter328Arg
NR_138151.2:n.1494T>A