Canonical Allele Identifier: CA445964705

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097458T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761758T>C , CM000667.2:g.110761758T>C	GRCh38
NC_000005.9:g.110097458T>C , CM000667.1:g.110097458T>C	GRCh37
NC_000005.8:g.110125357T>C	NCBI36
NG_051334.1:g.28623T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1233T>C MANE Select	ENSP00000348211.3:p.Ser411=
ENST00000355943.7:c.1233T>C	ENSP00000348211.3:p.Ser411=
ENST00000447245.6:c.990T>C	ENSP00000399717.2:p.Ser330=
ENST00000504098.1:c.795T>C	ENSP00000425708.1:p.Ser265=
ENST00000509432.1:c.594T>C	ENSP00000426604.1:p.Ser198=
ENST00000513706.2:n.2833T>C
ENST00000513807.5:c.747T>C	ENSP00000421134.1:p.Ser249=
NM_001303249.1:c.990T>C	NP_001290178.1:p.Ser330=
NM_001303250.1:c.960T>C	NP_001290179.1:p.Ser320=
NM_138773.2:c.1233T>C	NP_620128.1:p.Ser411=
NM_001303249.2:c.990T>C	NP_001290178.1:p.Ser330=
NM_001303250.2:c.960T>C	NP_001290179.1:p.Ser320=
NM_138773.3:c.1233T>C	NP_620128.1:p.Ser411=
NR_138151.1:n.1507T>C
NM_138773.4:c.1233T>C MANE Select	NP_620128.1:p.Ser411=
NM_001303249.3:c.990T>C	NP_001290178.1:p.Ser330=
NM_001303250.3:c.960T>C	NP_001290179.1:p.Ser320=
NR_138151.2:n.1472T>C