Canonical Allele Identifier: CA1406318439
Gene: SLC25A36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140963046_140963048delinsCTA , CM000665.2:g.140963046_140963048delinsCTA GRCh38
NC_000003.11:g.140681888_140681890delinsCTA , CM000665.1:g.140681888_140681890delinsCTA GRCh37
NC_000003.10:g.142164578_142164580delinsCTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000324194.12:c.285-81_285-79delinsCTA MANE Select ENSP00000320688.6:n.285-81_285-79delinsCTA
ENST00000648615.1:c.285-81_285-79delinsCTA ENSP00000497436.1:n.285-81_285-79delinsCTA
ENST00000324194.10:c.285-81_285-79delinsCTA ENSP00000320688.6:n.285-81_285-79delinsCTA
ENST00000393015.8:n.487-81_487-79delinsCTA
ENST00000446041.6:c.285-81_285-79delinsCTA ENSP00000401938.2:n.285-81_285-79delinsCTA
ENST00000453248.6:c.207-81_207-79delinsCTA ENSP00000391521.2:n.207-81_207-79delinsCTA
ENST00000502594.5:c.285-81_285-79delinsCTA ENSP00000423319.1:n.285-81_285-79delinsCTA
ENST00000507429.5:c.285-81_285-79delinsCTA ENSP00000421470.1:n.285-81_285-79delinsCTA
ENST00000512023.5:c.135-81_135-79delinsCTA ENSP00000424505.1:n.135-81_135-79delinsCTA
ENST00000512506.5:c.135-81_135-79delinsCTA ENSP00000423711.1:n.135-81_135-79delinsCTA
ENST00000513887.5:c.57-81_57-79delinsCTA ENSP00000422265.1:n.57-81_57-79delinsCTA
ENST00000515813.1:n.394-81_394-79delinsCTA
ENST00000631654.1:c.285-81_285-79delinsCTA ENSP00000487839.1:n.285-81_285-79delinsCTA
NM_001104647.1:c.285-81_285-79delinsCTA NP_001098117.1:n.285-81_285-79delinsCTA
NM_018155.2:c.285-81_285-79delinsCTA NP_060625.2:n.285-81_285-79delinsCTA
XM_011512951.1:c.381-81_381-79delinsCTA XP_011511253.1:n.381-81_381-79delinsCTA
XM_011512953.1:c.381-81_381-79delinsCTA XP_011511255.1:n.381-81_381-79delinsCTA
XR_924150.1:n.574-81_574-79delinsCTA
XR_924151.1:n.574-81_574-79delinsCTA
XR_924152.1:n.574-81_574-79delinsCTA
XR_924153.1:n.574-81_574-79delinsCTA
XR_924154.1:n.574-81_574-79delinsCTA
XR_924155.1:n.574-81_574-79delinsCTA
XR_924156.1:n.574-81_574-79delinsCTA
XR_924157.1:n.574-81_574-79delinsCTA
NM_001104647.3:c.285-81_285-79delinsCTA MANE Select NP_001098117.1:n.285-81_285-79delinsCTA
NM_018155.3:c.285-81_285-79delinsCTA NP_060625.2:n.285-81_285-79delinsCTA