Canonical Allele Identifier: CA2674823538

Gene: SLC25A46

Linked Data

• gnomAD v4: 5-110761066-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761066C>A , CM000667.2:g.110761066C>A	GRCh38
NC_000005.9:g.110096766C>A , CM000667.1:g.110096766C>A	GRCh37
NC_000005.8:g.110124665C>A	NCBI36
NG_051334.1:g.27931C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.679-138C>A MANE Select	ENSP00000348211.3:n.679-138C>A
ENST00000355943.7:c.679-138C>A	ENSP00000348211.3:n.679-138C>A
ENST00000447245.6:c.679-381C>A	ENSP00000399717.2:n.679-381C>A
ENST00000502462.6:n.995-138C>A
ENST00000504098.1:c.241-138C>A	ENSP00000425708.1:n.241-138C>A
ENST00000509432.1:c.40-138C>A	ENSP00000426604.1:n.40-138C>A
ENST00000513706.2:n.2279-138C>A
ENST00000513807.5:c.193-138C>A	ENSP00000421134.1:n.193-138C>A
NM_001303249.1:c.679-381C>A	NP_001290178.1:n.679-381C>A
NM_001303250.1:c.406-138C>A	NP_001290179.1:n.406-138C>A
NM_138773.2:c.679-138C>A	NP_620128.1:n.679-138C>A
NM_001303249.2:c.679-381C>A	NP_001290178.1:n.679-381C>A
NM_001303250.2:c.406-138C>A	NP_001290179.1:n.406-138C>A
NM_138773.3:c.679-138C>A	NP_620128.1:n.679-138C>A
NR_138151.1:n.953-138C>A
NM_138773.4:c.679-138C>A MANE Select	NP_620128.1:n.679-138C>A
NM_001303249.3:c.679-381C>A	NP_001290178.1:n.679-381C>A
NM_001303250.3:c.406-138C>A	NP_001290179.1:n.406-138C>A
NR_138151.2:n.918-138C>A