Canonical Allele Identifier: CA1572440028
Gene: SLC25A46 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110746277C= , CM000667.2:g.110746277C= GRCh38
NC_000005.9:g.110081978C= , CM000667.1:g.110081978C= GRCh37
NC_000005.8:g.110109877C= NCBI36
NG_051334.1:g.13142C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355943.8:c.393C= MANE Select ENSP00000348211.3:p.Tyr131=
ENST00000355943.7:c.393C= ENSP00000348211.3:p.Tyr131=
ENST00000447245.6:c.393C= ENSP00000399717.2:p.Tyr131=
ENST00000502462.6:n.709C=
ENST00000504098.1:c.-46C= ENSP00000425708.1:n.-46C=
ENST00000508781.5:n.222C=
ENST00000513807.5:c.-94C= ENSP00000421134.1:n.-94C=
NM_001303249.1:c.393C= NP_001290178.1:p.Tyr131=
NM_001303250.1:c.120C= NP_001290179.1:p.Tyr40=
NM_138773.2:c.393C= NP_620128.1:p.Tyr131=
XM_011543708.1:c.393C= XP_011542010.1:p.Tyr131=
NM_001303249.2:c.393C= NP_001290178.1:p.Tyr131=
NM_001303250.2:c.120C= NP_001290179.1:p.Tyr40=
NM_138773.3:c.393C= NP_620128.1:p.Tyr131=
NR_138151.1:n.541C=
NM_138773.4:c.393C= MANE Select NP_620128.1:p.Tyr131=
NM_001303249.3:c.393C= NP_001290178.1:p.Tyr131=
NM_001303250.3:c.120C= NP_001290179.1:p.Tyr40=
NR_138151.2:n.506C=
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