Canonical Allele Identifier: CA360697242

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097323T>A (hg19) ; chr5:g.110761623T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761623T>A , CM000667.2:g.110761623T>A	GRCh38
NC_000005.9:g.110097323T>A , CM000667.1:g.110097323T>A	GRCh37
NC_000005.8:g.110125222T>A	NCBI36
NG_051334.1:g.28488T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1098T>A MANE Select	ENSP00000348211.3:p.Tyr366Ter
ENST00000355943.7:c.1098T>A	ENSP00000348211.3:p.Tyr366Ter
ENST00000447245.6:c.855T>A	ENSP00000399717.2:p.Tyr285Ter
ENST00000502462.6:n.1414T>A
ENST00000504098.1:c.660T>A	ENSP00000425708.1:p.Tyr220Ter
ENST00000509432.1:c.459T>A	ENSP00000426604.1:p.Tyr153Ter
ENST00000513706.2:n.2698T>A
ENST00000513807.5:c.612T>A	ENSP00000421134.1:p.Tyr204Ter
NM_001303249.1:c.855T>A	NP_001290178.1:p.Tyr285Ter
NM_001303250.1:c.825T>A	NP_001290179.1:p.Tyr275Ter
NM_138773.2:c.1098T>A	NP_620128.1:p.Tyr366Ter
NM_001303249.2:c.855T>A	NP_001290178.1:p.Tyr285Ter
NM_001303250.2:c.825T>A	NP_001290179.1:p.Tyr275Ter
NM_138773.3:c.1098T>A	NP_620128.1:p.Tyr366Ter
NR_138151.1:n.1372T>A
NM_138773.4:c.1098T>A MANE Select	NP_620128.1:p.Tyr366Ter
NM_001303249.3:c.855T>A	NP_001290178.1:p.Tyr285Ter
NM_001303250.3:c.825T>A	NP_001290179.1:p.Tyr275Ter
NR_138151.2:n.1337T>A