Canonical Allele Identifier: CA2842090395

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761812A>G , CM000667.2:g.110761812A>G	GRCh38
NC_000005.9:g.110097512A>G , CM000667.1:g.110097512A>G	GRCh37
NC_000005.8:g.110125411A>G	NCBI36
NG_051334.1:g.28677A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.*30A>G MANE Select	ENSP00000348211.3:n.*30A>G
ENST00000355943.7:c.*30A>G	ENSP00000348211.3:n.*30A>G
ENST00000447245.6:c.*30A>G	ENSP00000399717.2:n.*30A>G
ENST00000504098.1:c.*30A>G	ENSP00000425708.1:n.*30A>G
ENST00000509432.1:c.*30A>G	ENSP00000426604.1:n.*30A>G
ENST00000513706.2:n.2887A>G
ENST00000513807.5:c.*30A>G	ENSP00000421134.1:n.*30A>G
NM_001303249.1:c.*30A>G	NP_001290178.1:n.*30A>G
NM_001303250.1:c.*30A>G	NP_001290179.1:n.*30A>G
NM_138773.2:c.*30A>G	NP_620128.1:n.*30A>G
NM_001303249.2:c.*30A>G	NP_001290178.1:n.*30A>G
NM_001303250.2:c.*30A>G	NP_001290179.1:n.*30A>G
NM_138773.3:c.*30A>G	NP_620128.1:n.*30A>G
NR_138151.1:n.1561A>G
NM_138773.4:c.*30A>G MANE Select	NP_620128.1:n.*30A>G
NM_001303249.3:c.*30A>G	NP_001290178.1:n.*30A>G
NM_001303250.3:c.*30A>G	NP_001290179.1:n.*30A>G
NR_138151.2:n.1526A>G