Canonical Allele Identifier: CA1572423221

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761225A= , CM000667.2:g.110761225A=	GRCh38
NC_000005.9:g.110096925A= , CM000667.1:g.110096925A=	GRCh37
NC_000005.8:g.110124824A=	NCBI36
NG_051334.1:g.28090A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.700A= MANE Select	ENSP00000348211.3:p.Thr234=
ENST00000355943.7:c.700A=	ENSP00000348211.3:p.Thr234=
ENST00000447245.6:c.679-222A=	ENSP00000399717.2:n.679-222A=
ENST00000502462.6:n.1016A=
ENST00000504098.1:c.262A=	ENSP00000425708.1:p.Thr88=
ENST00000509432.1:c.61A=	ENSP00000426604.1:p.Thr21=
ENST00000513706.2:n.2300A=
ENST00000513807.5:c.214A=	ENSP00000421134.1:p.Thr72=
NM_001303249.1:c.679-222A=	NP_001290178.1:n.679-222A=
NM_001303250.1:c.427A=	NP_001290179.1:p.Thr143=
NM_138773.2:c.700A=	NP_620128.1:p.Thr234=
NM_001303249.2:c.679-222A=	NP_001290178.1:n.679-222A=
NM_001303250.2:c.427A=	NP_001290179.1:p.Thr143=
NM_138773.3:c.700A=	NP_620128.1:p.Thr234=
NR_138151.1:n.974A=
NM_138773.4:c.700A= MANE Select	NP_620128.1:p.Thr234=
NM_001303249.3:c.679-222A=	NP_001290178.1:n.679-222A=
NM_001303250.3:c.427A=	NP_001290179.1:p.Thr143=
NR_138151.2:n.939A=