Canonical Allele Identifier: CA2842090396

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761813A>T , CM000667.2:g.110761813A>T	GRCh38
NC_000005.9:g.110097513A>T , CM000667.1:g.110097513A>T	GRCh37
NC_000005.8:g.110125412A>T	NCBI36
NG_051334.1:g.28678A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.*31A>T MANE Select	ENSP00000348211.3:n.*31A>T
ENST00000355943.7:c.*31A>T	ENSP00000348211.3:n.*31A>T
ENST00000447245.6:c.*31A>T	ENSP00000399717.2:n.*31A>T
ENST00000504098.1:c.*31A>T	ENSP00000425708.1:n.*31A>T
ENST00000509432.1:c.*31A>T	ENSP00000426604.1:n.*31A>T
ENST00000513706.2:n.2888A>T
ENST00000513807.5:c.*31A>T	ENSP00000421134.1:n.*31A>T
NM_001303249.1:c.*31A>T	NP_001290178.1:n.*31A>T
NM_001303250.1:c.*31A>T	NP_001290179.1:n.*31A>T
NM_138773.2:c.*31A>T	NP_620128.1:n.*31A>T
NM_001303249.2:c.*31A>T	NP_001290178.1:n.*31A>T
NM_001303250.2:c.*31A>T	NP_001290179.1:n.*31A>T
NM_138773.3:c.*31A>T	NP_620128.1:n.*31A>T
NR_138151.1:n.1562A>T
NM_138773.4:c.*31A>T MANE Select	NP_620128.1:n.*31A>T
NM_001303249.3:c.*31A>T	NP_001290178.1:n.*31A>T
NM_001303250.3:c.*31A>T	NP_001290179.1:n.*31A>T
NR_138151.2:n.1527A>T