Canonical Allele Identifier: CA1572423943

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761652T= , CM000667.2:g.110761652T=	GRCh38
NC_000005.9:g.110097352T= , CM000667.1:g.110097352T=	GRCh37
NC_000005.8:g.110125251T=	NCBI36
NG_051334.1:g.28517T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1127T= MANE Select	ENSP00000348211.3:p.Ile376=
ENST00000355943.7:c.1127T=	ENSP00000348211.3:p.Ile376=
ENST00000447245.6:c.884T=	ENSP00000399717.2:p.Ile295=
ENST00000502462.6:n.1443T=
ENST00000504098.1:c.689T=	ENSP00000425708.1:p.Ile230=
ENST00000509432.1:c.488T=	ENSP00000426604.1:p.Ile163=
ENST00000513706.2:n.2727T=
ENST00000513807.5:c.641T=	ENSP00000421134.1:p.Ile214=
NM_001303249.1:c.884T=	NP_001290178.1:p.Ile295=
NM_001303250.1:c.854T=	NP_001290179.1:p.Ile285=
NM_138773.2:c.1127T=	NP_620128.1:p.Ile376=
NM_001303249.2:c.884T=	NP_001290178.1:p.Ile295=
NM_001303250.2:c.854T=	NP_001290179.1:p.Ile285=
NM_138773.3:c.1127T=	NP_620128.1:p.Ile376=
NR_138151.1:n.1401T=
NM_138773.4:c.1127T= MANE Select	NP_620128.1:p.Ile376=
NM_001303249.3:c.884T=	NP_001290178.1:p.Ile295=
NM_001303250.3:c.854T=	NP_001290179.1:p.Ile285=
NR_138151.2:n.1366T=