Canonical Allele Identifier: CA1572424039

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761706T= , CM000667.2:g.110761706T=	GRCh38
NC_000005.9:g.110097406T= , CM000667.1:g.110097406T=	GRCh37
NC_000005.8:g.110125305T=	NCBI36
NG_051334.1:g.28571T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1181T= MANE Select	ENSP00000348211.3:p.Ile394=
ENST00000355943.7:c.1181T=	ENSP00000348211.3:p.Ile394=
ENST00000447245.6:c.938T=	ENSP00000399717.2:p.Ile313=
ENST00000504098.1:c.743T=	ENSP00000425708.1:p.Ile248=
ENST00000509432.1:c.542T=	ENSP00000426604.1:p.Ile181=
ENST00000513706.2:n.2781T=
ENST00000513807.5:c.695T=	ENSP00000421134.1:p.Ile232=
NM_001303249.1:c.938T=	NP_001290178.1:p.Ile313=
NM_001303250.1:c.908T=	NP_001290179.1:p.Ile303=
NM_138773.2:c.1181T=	NP_620128.1:p.Ile394=
NM_001303249.2:c.938T=	NP_001290178.1:p.Ile313=
NM_001303250.2:c.908T=	NP_001290179.1:p.Ile303=
NM_138773.3:c.1181T=	NP_620128.1:p.Ile394=
NR_138151.1:n.1455T=
NM_138773.4:c.1181T= MANE Select	NP_620128.1:p.Ile394=
NM_001303249.3:c.938T=	NP_001290178.1:p.Ile313=
NM_001303250.3:c.908T=	NP_001290179.1:p.Ile303=
NR_138151.2:n.1420T=