Canonical Allele Identifier: CA1572423646

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761452G= , CM000667.2:g.110761452G=	GRCh38
NC_000005.9:g.110097152G= , CM000667.1:g.110097152G=	GRCh37
NC_000005.8:g.110125051G=	NCBI36
NG_051334.1:g.28317G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355943.8:c.927G= MANE Select	ENSP00000348211.3:p.Met309=
ENST00000355943.7:c.927G=	ENSP00000348211.3:p.Met309=
ENST00000447245.6:c.684G=	ENSP00000399717.2:p.Met228=
ENST00000502462.6:n.1243G=
ENST00000504098.1:c.489G=	ENSP00000425708.1:p.Met163=
ENST00000509432.1:c.288G=	ENSP00000426604.1:p.Met96=
ENST00000513706.2:n.2527G=
ENST00000513807.5:c.441G=	ENSP00000421134.1:p.Met147=
NM_001303249.1:c.684G=	NP_001290178.1:p.Met228=
NM_001303250.1:c.654G=	NP_001290179.1:p.Met218=
NM_138773.2:c.927G=	NP_620128.1:p.Met309=
NM_001303249.2:c.684G=	NP_001290178.1:p.Met228=
NM_001303250.2:c.654G=	NP_001290179.1:p.Met218=
NM_138773.3:c.927G=	NP_620128.1:p.Met309=
NR_138151.1:n.1201G=
NM_138773.4:c.927G= MANE Select	NP_620128.1:p.Met309=
NM_001303249.3:c.684G=	NP_001290178.1:p.Met228=
NM_001303250.3:c.654G=	NP_001290179.1:p.Met218=
NR_138151.2:n.1166G=