Canonical Allele Identifier: CA360695972

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110096904A>G (hg19) ; chr5:g.110761204A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761204A>G , CM000667.2:g.110761204A>G	GRCh38
NC_000005.9:g.110096904A>G , CM000667.1:g.110096904A>G	GRCh37
NC_000005.8:g.110124803A>G	NCBI36
NG_051334.1:g.28069A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.679A>G MANE Select	ENSP00000348211.3:p.Ser227Gly
ENST00000355943.7:c.679A>G	ENSP00000348211.3:p.Ser227Gly
ENST00000447245.6:c.679-243A>G	ENSP00000399717.2:n.679-243A>G
ENST00000502462.6:n.995A>G
ENST00000504098.1:c.241A>G	ENSP00000425708.1:p.Ser81Gly
ENST00000509432.1:c.40A>G	ENSP00000426604.1:p.Ser14Gly
ENST00000513706.2:n.2279A>G
ENST00000513807.5:c.193A>G	ENSP00000421134.1:p.Ser65Gly
NM_001303249.1:c.679-243A>G	NP_001290178.1:n.679-243A>G
NM_001303250.1:c.406A>G	NP_001290179.1:p.Ser136Gly
NM_138773.2:c.679A>G	NP_620128.1:p.Ser227Gly
NM_001303249.2:c.679-243A>G	NP_001290178.1:n.679-243A>G
NM_001303250.2:c.406A>G	NP_001290179.1:p.Ser136Gly
NM_138773.3:c.679A>G	NP_620128.1:p.Ser227Gly
NR_138151.1:n.953A>G
NM_138773.4:c.679A>G MANE Select	NP_620128.1:p.Ser227Gly
NM_001303249.3:c.679-243A>G	NP_001290178.1:n.679-243A>G
NM_001303250.3:c.406A>G	NP_001290179.1:p.Ser136Gly
NR_138151.2:n.918A>G