Canonical Allele Identifier: CA360697621

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097387G>A (hg19) ; chr5:g.110761687G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761687G>A , CM000667.2:g.110761687G>A	GRCh38
NC_000005.9:g.110097387G>A , CM000667.1:g.110097387G>A	GRCh37
NC_000005.8:g.110125286G>A	NCBI36
NG_051334.1:g.28552G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1162G>A MANE Select	ENSP00000348211.3:p.Gly388Arg
ENST00000355943.7:c.1162G>A	ENSP00000348211.3:p.Gly388Arg
ENST00000447245.6:c.919G>A	ENSP00000399717.2:p.Gly307Arg
ENST00000504098.1:c.724G>A	ENSP00000425708.1:p.Gly242Arg
ENST00000509432.1:c.523G>A	ENSP00000426604.1:p.Gly175Arg
ENST00000513706.2:n.2762G>A
ENST00000513807.5:c.676G>A	ENSP00000421134.1:p.Gly226Arg
NM_001303249.1:c.919G>A	NP_001290178.1:p.Gly307Arg
NM_001303250.1:c.889G>A	NP_001290179.1:p.Gly297Arg
NM_138773.2:c.1162G>A	NP_620128.1:p.Gly388Arg
NM_001303249.2:c.919G>A	NP_001290178.1:p.Gly307Arg
NM_001303250.2:c.889G>A	NP_001290179.1:p.Gly297Arg
NM_138773.3:c.1162G>A	NP_620128.1:p.Gly388Arg
NR_138151.1:n.1436G>A
NM_138773.4:c.1162G>A MANE Select	NP_620128.1:p.Gly388Arg
NM_001303249.3:c.919G>A	NP_001290178.1:p.Gly307Arg
NM_001303250.3:c.889G>A	NP_001290179.1:p.Gly297Arg
NR_138151.2:n.1401G>A