Canonical Allele Identifier: CA360697211

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097318C>T (hg19) ; chr5:g.110761618C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761618C>T , CM000667.2:g.110761618C>T	GRCh38
NC_000005.9:g.110097318C>T , CM000667.1:g.110097318C>T	GRCh37
NC_000005.8:g.110125217C>T	NCBI36
NG_051334.1:g.28483C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1093C>T MANE Select	ENSP00000348211.3:p.Gln365Ter
ENST00000355943.7:c.1093C>T	ENSP00000348211.3:p.Gln365Ter
ENST00000447245.6:c.850C>T	ENSP00000399717.2:p.Gln284Ter
ENST00000502462.6:n.1409C>T
ENST00000504098.1:c.655C>T	ENSP00000425708.1:p.Gln219Ter
ENST00000509432.1:c.454C>T	ENSP00000426604.1:p.Gln152Ter
ENST00000513706.2:n.2693C>T
ENST00000513807.5:c.607C>T	ENSP00000421134.1:p.Gln203Ter
NM_001303249.1:c.850C>T	NP_001290178.1:p.Gln284Ter
NM_001303250.1:c.820C>T	NP_001290179.1:p.Gln274Ter
NM_138773.2:c.1093C>T	NP_620128.1:p.Gln365Ter
NM_001303249.2:c.850C>T	NP_001290178.1:p.Gln284Ter
NM_001303250.2:c.820C>T	NP_001290179.1:p.Gln274Ter
NM_138773.3:c.1093C>T	NP_620128.1:p.Gln365Ter
NR_138151.1:n.1367C>T
NM_138773.4:c.1093C>T MANE Select	NP_620128.1:p.Gln365Ter
NM_001303249.3:c.850C>T	NP_001290178.1:p.Gln284Ter
NM_001303250.3:c.820C>T	NP_001290179.1:p.Gln274Ter
NR_138151.2:n.1332C>T