Canonical Allele Identifier: CA1572423258

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761256T= , CM000667.2:g.110761256T=	GRCh38
NC_000005.9:g.110096956T= , CM000667.1:g.110096956T=	GRCh37
NC_000005.8:g.110124855T=	NCBI36
NG_051334.1:g.28121T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.731T= MANE Select	ENSP00000348211.3:p.Ile244=
ENST00000355943.7:c.731T=	ENSP00000348211.3:p.Ile244=
ENST00000447245.6:c.679-191T=	ENSP00000399717.2:n.679-191T=
ENST00000502462.6:n.1047T=
ENST00000504098.1:c.293T=	ENSP00000425708.1:p.Ile98=
ENST00000509432.1:c.92T=	ENSP00000426604.1:p.Ile31=
ENST00000513706.2:n.2331T=
ENST00000513807.5:c.245T=	ENSP00000421134.1:p.Ile82=
NM_001303249.1:c.679-191T=	NP_001290178.1:n.679-191T=
NM_001303250.1:c.458T=	NP_001290179.1:p.Ile153=
NM_138773.2:c.731T=	NP_620128.1:p.Ile244=
NM_001303249.2:c.679-191T=	NP_001290178.1:n.679-191T=
NM_001303250.2:c.458T=	NP_001290179.1:p.Ile153=
NM_138773.3:c.731T=	NP_620128.1:p.Ile244=
NR_138151.1:n.1005T=
NM_138773.4:c.731T= MANE Select	NP_620128.1:p.Ile244=
NM_001303249.3:c.679-191T=	NP_001290178.1:n.679-191T=
NM_001303250.3:c.458T=	NP_001290179.1:p.Ile153=
NR_138151.2:n.970T=