Canonical Allele Identifier: CA360696081

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110096953G>T (hg19) ; chr5:g.110761253G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761253G>T , CM000667.2:g.110761253G>T	GRCh38
NC_000005.9:g.110096953G>T , CM000667.1:g.110096953G>T	GRCh37
NC_000005.8:g.110124852G>T	NCBI36
NG_051334.1:g.28118G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.728G>T MANE Select	ENSP00000348211.3:p.Gly243Val
ENST00000355943.7:c.728G>T	ENSP00000348211.3:p.Gly243Val
ENST00000447245.6:c.679-194G>T	ENSP00000399717.2:n.679-194G>T
ENST00000502462.6:n.1044G>T
ENST00000504098.1:c.290G>T	ENSP00000425708.1:p.Gly97Val
ENST00000509432.1:c.89G>T	ENSP00000426604.1:p.Gly30Val
ENST00000513706.2:n.2328G>T
ENST00000513807.5:c.242G>T	ENSP00000421134.1:p.Gly81Val
NM_001303249.1:c.679-194G>T	NP_001290178.1:n.679-194G>T
NM_001303250.1:c.455G>T	NP_001290179.1:p.Gly152Val
NM_138773.2:c.728G>T	NP_620128.1:p.Gly243Val
NM_001303249.2:c.679-194G>T	NP_001290178.1:n.679-194G>T
NM_001303250.2:c.455G>T	NP_001290179.1:p.Gly152Val
NM_138773.3:c.728G>T	NP_620128.1:p.Gly243Val
NR_138151.1:n.1002G>T
NM_138773.4:c.728G>T MANE Select	NP_620128.1:p.Gly243Val
NM_001303249.3:c.679-194G>T	NP_001290178.1:n.679-194G>T
NM_001303250.3:c.455G>T	NP_001290179.1:p.Gly152Val
NR_138151.2:n.967G>T