Canonical Allele Identifier: CA1572423667

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761456G= , CM000667.2:g.110761456G=	GRCh38
NC_000005.9:g.110097156G= , CM000667.1:g.110097156G=	GRCh37
NC_000005.8:g.110125055G=	NCBI36
NG_051334.1:g.28321G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355943.8:c.931G= MANE Select	ENSP00000348211.3:p.Asp311=
ENST00000355943.7:c.931G=	ENSP00000348211.3:p.Asp311=
ENST00000447245.6:c.688G=	ENSP00000399717.2:p.Asp230=
ENST00000502462.6:n.1247G=
ENST00000504098.1:c.493G=	ENSP00000425708.1:p.Asp165=
ENST00000509432.1:c.292G=	ENSP00000426604.1:p.Asp98=
ENST00000513706.2:n.2531G=
ENST00000513807.5:c.445G=	ENSP00000421134.1:p.Asp149=
NM_001303249.1:c.688G=	NP_001290178.1:p.Asp230=
NM_001303250.1:c.658G=	NP_001290179.1:p.Asp220=
NM_138773.2:c.931G=	NP_620128.1:p.Asp311=
NM_001303249.2:c.688G=	NP_001290178.1:p.Asp230=
NM_001303250.2:c.658G=	NP_001290179.1:p.Asp220=
NM_138773.3:c.931G=	NP_620128.1:p.Asp311=
NR_138151.1:n.1205G=
NM_138773.4:c.931G= MANE Select	NP_620128.1:p.Asp311=
NM_001303249.3:c.688G=	NP_001290178.1:p.Asp230=
NM_001303250.3:c.658G=	NP_001290179.1:p.Asp220=
NR_138151.2:n.1170G=