Canonical Allele Identifier: CA1572424078

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761735C= , CM000667.2:g.110761735C=	GRCh38
NC_000005.9:g.110097435C= , CM000667.1:g.110097435C=	GRCh37
NC_000005.8:g.110125334C=	NCBI36
NG_051334.1:g.28600C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1210C= MANE Select	ENSP00000348211.3:p.Gln404=
ENST00000355943.7:c.1210C=	ENSP00000348211.3:p.Gln404=
ENST00000447245.6:c.967C=	ENSP00000399717.2:p.Gln323=
ENST00000504098.1:c.772C=	ENSP00000425708.1:p.Gln258=
ENST00000509432.1:c.571C=	ENSP00000426604.1:p.Gln191=
ENST00000513706.2:n.2810C=
ENST00000513807.5:c.724C=	ENSP00000421134.1:p.Gln242=
NM_001303249.1:c.967C=	NP_001290178.1:p.Gln323=
NM_001303250.1:c.937C=	NP_001290179.1:p.Gln313=
NM_138773.2:c.1210C=	NP_620128.1:p.Gln404=
NM_001303249.2:c.967C=	NP_001290178.1:p.Gln323=
NM_001303250.2:c.937C=	NP_001290179.1:p.Gln313=
NM_138773.3:c.1210C=	NP_620128.1:p.Gln404=
NR_138151.1:n.1484C=
NM_138773.4:c.1210C= MANE Select	NP_620128.1:p.Gln404=
NM_001303249.3:c.967C=	NP_001290178.1:p.Gln323=
NM_001303250.3:c.937C=	NP_001290179.1:p.Gln313=
NR_138151.2:n.1449C=