Canonical Allele Identifier: CA1572424216

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761824G= , CM000667.2:g.110761824G=	GRCh38
NC_000005.9:g.110097524G= , CM000667.1:g.110097524G=	GRCh37
NC_000005.8:g.110125423G=	NCBI36
NG_051334.1:g.28689G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.*42G= MANE Select	ENSP00000348211.3:n.*42G=
ENST00000355943.7:c.*42G=	ENSP00000348211.3:n.*42G=
ENST00000447245.6:c.*42G=	ENSP00000399717.2:n.*42G=
ENST00000504098.1:c.*42G=	ENSP00000425708.1:n.*42G=
ENST00000509432.1:c.*42G=	ENSP00000426604.1:n.*42G=
ENST00000513706.2:n.2899G=
ENST00000513807.5:c.*42G=	ENSP00000421134.1:n.*42G=
NM_001303249.1:c.*42G=	NP_001290178.1:n.*42G=
NM_001303250.1:c.*42G=	NP_001290179.1:n.*42G=
NM_138773.2:c.*42G=	NP_620128.1:n.*42G=
NM_001303249.2:c.*42G=	NP_001290178.1:n.*42G=
NM_001303250.2:c.*42G=	NP_001290179.1:n.*42G=
NM_138773.3:c.*42G=	NP_620128.1:n.*42G=
NR_138151.1:n.1573G=
NM_138773.4:c.*42G= MANE Select	NP_620128.1:n.*42G=
NM_001303249.3:c.*42G=	NP_001290178.1:n.*42G=
NM_001303250.3:c.*42G=	NP_001290179.1:n.*42G=
NR_138151.2:n.1538G=