Canonical Allele Identifier: CA360697185

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097314T>A (hg19) ; chr5:g.110761614T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761614T>A , CM000667.2:g.110761614T>A	GRCh38
NC_000005.9:g.110097314T>A , CM000667.1:g.110097314T>A	GRCh37
NC_000005.8:g.110125213T>A	NCBI36
NG_051334.1:g.28479T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1089T>A MANE Select	ENSP00000348211.3:p.Asn363Lys
ENST00000355943.7:c.1089T>A	ENSP00000348211.3:p.Asn363Lys
ENST00000447245.6:c.846T>A	ENSP00000399717.2:p.Asn282Lys
ENST00000502462.6:n.1405T>A
ENST00000504098.1:c.651T>A	ENSP00000425708.1:p.Asn217Lys
ENST00000509432.1:c.450T>A	ENSP00000426604.1:p.Asn150Lys
ENST00000513706.2:n.2689T>A
ENST00000513807.5:c.603T>A	ENSP00000421134.1:p.Asn201Lys
NM_001303249.1:c.846T>A	NP_001290178.1:p.Asn282Lys
NM_001303250.1:c.816T>A	NP_001290179.1:p.Asn272Lys
NM_138773.2:c.1089T>A	NP_620128.1:p.Asn363Lys
NM_001303249.2:c.846T>A	NP_001290178.1:p.Asn282Lys
NM_001303250.2:c.816T>A	NP_001290179.1:p.Asn272Lys
NM_138773.3:c.1089T>A	NP_620128.1:p.Asn363Lys
NR_138151.1:n.1363T>A
NM_138773.4:c.1089T>A MANE Select	NP_620128.1:p.Asn363Lys
NM_001303249.3:c.846T>A	NP_001290178.1:p.Asn282Lys
NM_001303250.3:c.816T>A	NP_001290179.1:p.Asn272Lys
NR_138151.2:n.1328T>A