Canonical Allele Identifier: CA360696510

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097160C>A (hg19) ; chr5:g.110761460C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761460C>A , CM000667.2:g.110761460C>A	GRCh38
NC_000005.9:g.110097160C>A , CM000667.1:g.110097160C>A	GRCh37
NC_000005.8:g.110125059C>A	NCBI36
NG_051334.1:g.28325C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355943.8:c.935C>A MANE Select	ENSP00000348211.3:p.Ala312Asp
ENST00000355943.7:c.935C>A	ENSP00000348211.3:p.Ala312Asp
ENST00000447245.6:c.692C>A	ENSP00000399717.2:p.Ala231Asp
ENST00000502462.6:n.1251C>A
ENST00000504098.1:c.497C>A	ENSP00000425708.1:p.Ala166Asp
ENST00000509432.1:c.296C>A	ENSP00000426604.1:p.Ala99Asp
ENST00000513706.2:n.2535C>A
ENST00000513807.5:c.449C>A	ENSP00000421134.1:p.Ala150Asp
NM_001303249.1:c.692C>A	NP_001290178.1:p.Ala231Asp
NM_001303250.1:c.662C>A	NP_001290179.1:p.Ala221Asp
NM_138773.2:c.935C>A	NP_620128.1:p.Ala312Asp
NM_001303249.2:c.692C>A	NP_001290178.1:p.Ala231Asp
NM_001303250.2:c.662C>A	NP_001290179.1:p.Ala221Asp
NM_138773.3:c.935C>A	NP_620128.1:p.Ala312Asp
NR_138151.1:n.1209C>A
NM_138773.4:c.935C>A MANE Select	NP_620128.1:p.Ala312Asp
NM_001303249.3:c.692C>A	NP_001290178.1:p.Ala231Asp
NM_001303250.3:c.662C>A	NP_001290179.1:p.Ala221Asp
NR_138151.2:n.1174C>A