Canonical Allele Identifier: CA354858086
Gene: SLC25A36 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140963185C>A , CM000665.2:g.140963185C>A GRCh38
NC_000003.11:g.140682027C>A , CM000665.1:g.140682027C>A GRCh37
NC_000003.10:g.142164717C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000324194.12:c.343C>A MANE Select ENSP00000320688.6:p.Pro115Thr
ENST00000648615.1:c.343C>A ENSP00000497436.1:p.Pro115Thr
ENST00000324194.10:c.343C>A ENSP00000320688.6:p.Pro115Thr
ENST00000393015.8:n.545C>A
ENST00000446041.6:c.343C>A ENSP00000401938.2:p.Pro115Thr
ENST00000453248.6:c.265C>A ENSP00000391521.2:p.Pro89Thr
ENST00000502594.5:c.343C>A ENSP00000423319.1:p.Pro115Thr
ENST00000507429.5:c.343C>A ENSP00000421470.1:p.Pro115Thr
ENST00000512023.5:c.193C>A ENSP00000424505.1:p.Pro65Thr
ENST00000512506.5:c.193C>A ENSP00000423711.1:p.Pro65Thr
ENST00000513887.5:c.115C>A ENSP00000422265.1:p.Pro39Thr
ENST00000515813.1:n.452C>A
ENST00000631654.1:c.343C>A ENSP00000487839.1:p.Pro115Thr
NM_001104647.1:c.343C>A NP_001098117.1:p.Pro115Thr
NM_018155.2:c.343C>A NP_060625.2:p.Pro115Thr
XM_006713685.2:c.-764C>A XP_006713748.1:n.-764C>A
XM_011512951.1:c.439C>A XP_011511253.1:p.Pro147Thr
XM_011512952.1:c.-112C>A XP_011511254.1:n.-112C>A
XM_011512953.1:c.439C>A XP_011511255.1:p.Pro147Thr
XR_924150.1:n.632C>A
XR_924151.1:n.632C>A
XR_924152.1:n.632C>A
XR_924153.1:n.632C>A
XR_924154.1:n.632C>A
XR_924155.1:n.632C>A
XR_924156.1:n.632C>A
XR_924157.1:n.632C>A
NM_001104647.3:c.343C>A MANE Select NP_001098117.1:p.Pro115Thr
NM_018155.3:c.343C>A NP_060625.2:p.Pro115Thr