Canonical Allele Identifier: CA360696005

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110096920A>G (hg19) ; chr5:g.110761220A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761220A>G , CM000667.2:g.110761220A>G	GRCh38
NC_000005.9:g.110096920A>G , CM000667.1:g.110096920A>G	GRCh37
NC_000005.8:g.110124819A>G	NCBI36
NG_051334.1:g.28085A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.695A>G MANE Select	ENSP00000348211.3:p.Asp232Gly
ENST00000355943.7:c.695A>G	ENSP00000348211.3:p.Asp232Gly
ENST00000447245.6:c.679-227A>G	ENSP00000399717.2:n.679-227A>G
ENST00000502462.6:n.1011A>G
ENST00000504098.1:c.257A>G	ENSP00000425708.1:p.Asp86Gly
ENST00000509432.1:c.56A>G	ENSP00000426604.1:p.Asp19Gly
ENST00000513706.2:n.2295A>G
ENST00000513807.5:c.209A>G	ENSP00000421134.1:p.Asp70Gly
NM_001303249.1:c.679-227A>G	NP_001290178.1:n.679-227A>G
NM_001303250.1:c.422A>G	NP_001290179.1:p.Asp141Gly
NM_138773.2:c.695A>G	NP_620128.1:p.Asp232Gly
NM_001303249.2:c.679-227A>G	NP_001290178.1:n.679-227A>G
NM_001303250.2:c.422A>G	NP_001290179.1:p.Asp141Gly
NM_138773.3:c.695A>G	NP_620128.1:p.Asp232Gly
NR_138151.1:n.969A>G
NM_138773.4:c.695A>G MANE Select	NP_620128.1:p.Asp232Gly
NM_001303249.3:c.679-227A>G	NP_001290178.1:n.679-227A>G
NM_001303250.3:c.422A>G	NP_001290179.1:p.Asp141Gly
NR_138151.2:n.934A>G