Canonical Allele Identifier: CA1572424056

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761723G= , CM000667.2:g.110761723G=	GRCh38
NC_000005.9:g.110097423G= , CM000667.1:g.110097423G=	GRCh37
NC_000005.8:g.110125322G=	NCBI36
NG_051334.1:g.28588G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1198G= MANE Select	ENSP00000348211.3:p.Ala400=
ENST00000355943.7:c.1198G=	ENSP00000348211.3:p.Ala400=
ENST00000447245.6:c.955G=	ENSP00000399717.2:p.Ala319=
ENST00000504098.1:c.760G=	ENSP00000425708.1:p.Ala254=
ENST00000509432.1:c.559G=	ENSP00000426604.1:p.Ala187=
ENST00000513706.2:n.2798G=
ENST00000513807.5:c.712G=	ENSP00000421134.1:p.Ala238=
NM_001303249.1:c.955G=	NP_001290178.1:p.Ala319=
NM_001303250.1:c.925G=	NP_001290179.1:p.Ala309=
NM_138773.2:c.1198G=	NP_620128.1:p.Ala400=
NM_001303249.2:c.955G=	NP_001290178.1:p.Ala319=
NM_001303250.2:c.925G=	NP_001290179.1:p.Ala309=
NM_138773.3:c.1198G=	NP_620128.1:p.Ala400=
NR_138151.1:n.1472G=
NM_138773.4:c.1198G= MANE Select	NP_620128.1:p.Ala400=
NM_001303249.3:c.955G=	NP_001290178.1:p.Ala319=
NM_001303250.3:c.925G=	NP_001290179.1:p.Ala309=
NR_138151.2:n.1437G=