Canonical Allele Identifier: CA1572423910

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761617A= , CM000667.2:g.110761617A=	GRCh38
NC_000005.9:g.110097317A= , CM000667.1:g.110097317A=	GRCh37
NC_000005.8:g.110125216A=	NCBI36
NG_051334.1:g.28482A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1092A= MANE Select	ENSP00000348211.3:p.Thr364=
ENST00000355943.7:c.1092A=	ENSP00000348211.3:p.Thr364=
ENST00000447245.6:c.849A=	ENSP00000399717.2:p.Thr283=
ENST00000502462.6:n.1408A=
ENST00000504098.1:c.654A=	ENSP00000425708.1:p.Thr218=
ENST00000509432.1:c.453A=	ENSP00000426604.1:p.Thr151=
ENST00000513706.2:n.2692A=
ENST00000513807.5:c.606A=	ENSP00000421134.1:p.Thr202=
NM_001303249.1:c.849A=	NP_001290178.1:p.Thr283=
NM_001303250.1:c.819A=	NP_001290179.1:p.Thr273=
NM_138773.2:c.1092A=	NP_620128.1:p.Thr364=
NM_001303249.2:c.849A=	NP_001290178.1:p.Thr283=
NM_001303250.2:c.819A=	NP_001290179.1:p.Thr273=
NM_138773.3:c.1092A=	NP_620128.1:p.Thr364=
NR_138151.1:n.1366A=
NM_138773.4:c.1092A= MANE Select	NP_620128.1:p.Thr364=
NM_001303249.3:c.849A=	NP_001290178.1:p.Thr283=
NM_001303250.3:c.819A=	NP_001290179.1:p.Thr273=
NR_138151.2:n.1331A=