Canonical Allele Identifier: CA1572423263

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761258G= , CM000667.2:g.110761258G=	GRCh38
NC_000005.9:g.110096958G= , CM000667.1:g.110096958G=	GRCh37
NC_000005.8:g.110124857G=	NCBI36
NG_051334.1:g.28123G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.733G= MANE Select	ENSP00000348211.3:p.Gly245=
ENST00000355943.7:c.733G=	ENSP00000348211.3:p.Gly245=
ENST00000447245.6:c.679-189G=	ENSP00000399717.2:n.679-189G=
ENST00000502462.6:n.1049G=
ENST00000504098.1:c.295G=	ENSP00000425708.1:p.Gly99=
ENST00000509432.1:c.94G=	ENSP00000426604.1:p.Gly32=
ENST00000513706.2:n.2333G=
ENST00000513807.5:c.247G=	ENSP00000421134.1:p.Gly83=
NM_001303249.1:c.679-189G=	NP_001290178.1:n.679-189G=
NM_001303250.1:c.460G=	NP_001290179.1:p.Gly154=
NM_138773.2:c.733G=	NP_620128.1:p.Gly245=
NM_001303249.2:c.679-189G=	NP_001290178.1:n.679-189G=
NM_001303250.2:c.460G=	NP_001290179.1:p.Gly154=
NM_138773.3:c.733G=	NP_620128.1:p.Gly245=
NR_138151.1:n.1007G=
NM_138773.4:c.733G= MANE Select	NP_620128.1:p.Gly245=
NM_001303249.3:c.679-189G=	NP_001290178.1:n.679-189G=
NM_001303250.3:c.460G=	NP_001290179.1:p.Gly154=
NR_138151.2:n.972G=