Canonical Allele Identifier: CA360697572

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097376G>A (hg19) ; chr5:g.110761676G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761676G>A , CM000667.2:g.110761676G>A	GRCh38
NC_000005.9:g.110097376G>A , CM000667.1:g.110097376G>A	GRCh37
NC_000005.8:g.110125275G>A	NCBI36
NG_051334.1:g.28541G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1151G>A MANE Select	ENSP00000348211.3:p.Gly384Asp
ENST00000355943.7:c.1151G>A	ENSP00000348211.3:p.Gly384Asp
ENST00000447245.6:c.908G>A	ENSP00000399717.2:p.Gly303Asp
ENST00000504098.1:c.713G>A	ENSP00000425708.1:p.Gly238Asp
ENST00000509432.1:c.512G>A	ENSP00000426604.1:p.Gly171Asp
ENST00000513706.2:n.2751G>A
ENST00000513807.5:c.665G>A	ENSP00000421134.1:p.Gly222Asp
NM_001303249.1:c.908G>A	NP_001290178.1:p.Gly303Asp
NM_001303250.1:c.878G>A	NP_001290179.1:p.Gly293Asp
NM_138773.2:c.1151G>A	NP_620128.1:p.Gly384Asp
NM_001303249.2:c.908G>A	NP_001290178.1:p.Gly303Asp
NM_001303250.2:c.878G>A	NP_001290179.1:p.Gly293Asp
NM_138773.3:c.1151G>A	NP_620128.1:p.Gly384Asp
NR_138151.1:n.1425G>A
NM_138773.4:c.1151G>A MANE Select	NP_620128.1:p.Gly384Asp
NM_001303249.3:c.908G>A	NP_001290178.1:p.Gly303Asp
NM_001303250.3:c.878G>A	NP_001290179.1:p.Gly293Asp
NR_138151.2:n.1390G>A