Canonical Allele Identifier: CA1572423364

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761295G= , CM000667.2:g.110761295G=	GRCh38
NC_000005.9:g.110096995G= , CM000667.1:g.110096995G=	GRCh37
NC_000005.8:g.110124894G=	NCBI36
NG_051334.1:g.28160G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.770G= MANE Select	ENSP00000348211.3:p.Arg257=
ENST00000355943.7:c.770G=	ENSP00000348211.3:p.Arg257=
ENST00000447245.6:c.679-152G=	ENSP00000399717.2:n.679-152G=
ENST00000502462.6:n.1086G=
ENST00000504098.1:c.332G=	ENSP00000425708.1:p.Arg111=
ENST00000509432.1:c.131G=	ENSP00000426604.1:p.Arg44=
ENST00000513706.2:n.2370G=
ENST00000513807.5:c.284G=	ENSP00000421134.1:p.Arg95=
NM_001303249.1:c.679-152G=	NP_001290178.1:n.679-152G=
NM_001303250.1:c.497G=	NP_001290179.1:p.Arg166=
NM_138773.2:c.770G=	NP_620128.1:p.Arg257=
NM_001303249.2:c.679-152G=	NP_001290178.1:n.679-152G=
NM_001303250.2:c.497G=	NP_001290179.1:p.Arg166=
NM_138773.3:c.770G=	NP_620128.1:p.Arg257=
NR_138151.1:n.1044G=
NM_138773.4:c.770G= MANE Select	NP_620128.1:p.Arg257=
NM_001303249.3:c.679-152G=	NP_001290178.1:n.679-152G=
NM_001303250.3:c.497G=	NP_001290179.1:p.Arg166=
NR_138151.2:n.1009G=