Canonical Allele Identifier: CA360697050

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097291G>A (hg19) ; chr5:g.110761591G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761591G>A , CM000667.2:g.110761591G>A	GRCh38
NC_000005.9:g.110097291G>A , CM000667.1:g.110097291G>A	GRCh37
NC_000005.8:g.110125190G>A	NCBI36
NG_051334.1:g.28456G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1066G>A MANE Select	ENSP00000348211.3:p.Gly356Ser
ENST00000355943.7:c.1066G>A	ENSP00000348211.3:p.Gly356Ser
ENST00000447245.6:c.823G>A	ENSP00000399717.2:p.Gly275Ser
ENST00000502462.6:n.1382G>A
ENST00000504098.1:c.628G>A	ENSP00000425708.1:p.Gly210Ser
ENST00000509432.1:c.427G>A	ENSP00000426604.1:p.Gly143Ser
ENST00000513706.2:n.2666G>A
ENST00000513807.5:c.580G>A	ENSP00000421134.1:p.Gly194Ser
NM_001303249.1:c.823G>A	NP_001290178.1:p.Gly275Ser
NM_001303250.1:c.793G>A	NP_001290179.1:p.Gly265Ser
NM_138773.2:c.1066G>A	NP_620128.1:p.Gly356Ser
NM_001303249.2:c.823G>A	NP_001290178.1:p.Gly275Ser
NM_001303250.2:c.793G>A	NP_001290179.1:p.Gly265Ser
NM_138773.3:c.1066G>A	NP_620128.1:p.Gly356Ser
NR_138151.1:n.1340G>A
NM_138773.4:c.1066G>A MANE Select	NP_620128.1:p.Gly356Ser
NM_001303249.3:c.823G>A	NP_001290178.1:p.Gly275Ser
NM_001303250.3:c.793G>A	NP_001290179.1:p.Gly265Ser
NR_138151.2:n.1305G>A