Canonical Allele Identifier: CA1572424052

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761719G= , CM000667.2:g.110761719G=	GRCh38
NC_000005.9:g.110097419G= , CM000667.1:g.110097419G=	GRCh37
NC_000005.8:g.110125318G=	NCBI36
NG_051334.1:g.28584G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1194G= MANE Select	ENSP00000348211.3:p.Leu398=
ENST00000355943.7:c.1194G=	ENSP00000348211.3:p.Leu398=
ENST00000447245.6:c.951G=	ENSP00000399717.2:p.Leu317=
ENST00000504098.1:c.756G=	ENSP00000425708.1:p.Leu252=
ENST00000509432.1:c.555G=	ENSP00000426604.1:p.Leu185=
ENST00000513706.2:n.2794G=
ENST00000513807.5:c.708G=	ENSP00000421134.1:p.Leu236=
NM_001303249.1:c.951G=	NP_001290178.1:p.Leu317=
NM_001303250.1:c.921G=	NP_001290179.1:p.Leu307=
NM_138773.2:c.1194G=	NP_620128.1:p.Leu398=
NM_001303249.2:c.951G=	NP_001290178.1:p.Leu317=
NM_001303250.2:c.921G=	NP_001290179.1:p.Leu307=
NM_138773.3:c.1194G=	NP_620128.1:p.Leu398=
NR_138151.1:n.1468G=
NM_138773.4:c.1194G= MANE Select	NP_620128.1:p.Leu398=
NM_001303249.3:c.951G=	NP_001290178.1:p.Leu317=
NM_001303250.3:c.921G=	NP_001290179.1:p.Leu307=
NR_138151.2:n.1433G=