Canonical Allele Identifier: CA1572422990

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761015G= , CM000667.2:g.110761015G=	GRCh38
NC_000005.9:g.110096715G= , CM000667.1:g.110096715G=	GRCh37
NC_000005.8:g.110124614G=	NCBI36
NG_051334.1:g.27880G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.679-189G= MANE Select	ENSP00000348211.3:n.679-189G=
ENST00000355943.7:c.679-189G=	ENSP00000348211.3:n.679-189G=
ENST00000447245.6:c.679-432G=	ENSP00000399717.2:n.679-432G=
ENST00000502462.6:n.995-189G=
ENST00000504098.1:c.241-189G=	ENSP00000425708.1:n.241-189G=
ENST00000509432.1:c.40-189G=	ENSP00000426604.1:n.40-189G=
ENST00000513706.2:n.2279-189G=
ENST00000513807.5:c.193-189G=	ENSP00000421134.1:n.193-189G=
NM_001303249.1:c.679-432G=	NP_001290178.1:n.679-432G=
NM_001303250.1:c.406-189G=	NP_001290179.1:n.406-189G=
NM_138773.2:c.679-189G=	NP_620128.1:n.679-189G=
NM_001303249.2:c.679-432G=	NP_001290178.1:n.679-432G=
NM_001303250.2:c.406-189G=	NP_001290179.1:n.406-189G=
NM_138773.3:c.679-189G=	NP_620128.1:n.679-189G=
NR_138151.1:n.953-189G=
NM_138773.4:c.679-189G= MANE Select	NP_620128.1:n.679-189G=
NM_001303249.3:c.679-432G=	NP_001290178.1:n.679-432G=
NM_001303250.3:c.406-189G=	NP_001290179.1:n.406-189G=
NR_138151.2:n.918-189G=