Canonical Allele Identifier: CA1572440029
Gene: SLC25A46 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110746280T= , CM000667.2:g.110746280T= GRCh38
NC_000005.9:g.110081981T= , CM000667.1:g.110081981T= GRCh37
NC_000005.8:g.110109880T= NCBI36
NG_051334.1:g.13145T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355943.8:c.396T= MANE Select ENSP00000348211.3:p.His132=
ENST00000355943.7:c.396T= ENSP00000348211.3:p.His132=
ENST00000447245.6:c.396T= ENSP00000399717.2:p.His132=
ENST00000502462.6:n.712T=
ENST00000504098.1:c.-43T= ENSP00000425708.1:n.-43T=
ENST00000508781.5:n.225T=
ENST00000513807.5:c.-91T= ENSP00000421134.1:n.-91T=
NM_001303249.1:c.396T= NP_001290178.1:p.His132=
NM_001303250.1:c.123T= NP_001290179.1:p.His41=
NM_138773.2:c.396T= NP_620128.1:p.His132=
XM_011543708.1:c.396T= XP_011542010.1:p.His132=
NM_001303249.2:c.396T= NP_001290178.1:p.His132=
NM_001303250.2:c.123T= NP_001290179.1:p.His41=
NM_138773.3:c.396T= NP_620128.1:p.His132=
NR_138151.1:n.544T=
NM_138773.4:c.396T= MANE Select NP_620128.1:p.His132=
NM_001303249.3:c.396T= NP_001290178.1:p.His132=
NM_001303250.3:c.123T= NP_001290179.1:p.His41=
NR_138151.2:n.509T=
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