Canonical Allele Identifier: CA1054265854
Gene: SLC25A36 HGNC NCBI

Linked Data

dbSNP Id: rs1401285765

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140963264C>T , CM000665.2:g.140963264C>T GRCh38
NC_000003.11:g.140682106C>T , CM000665.1:g.140682106C>T GRCh37
NC_000003.10:g.142164796C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000324194.12:c.385+37C>T MANE Select ENSP00000320688.6:n.385+37C>T
ENST00000648615.1:c.385+37C>T ENSP00000497436.1:n.385+37C>T
ENST00000324194.10:c.385+37C>T ENSP00000320688.6:n.385+37C>T
ENST00000393015.8:n.587+37C>T
ENST00000446041.6:c.385+37C>T ENSP00000401938.2:n.385+37C>T
ENST00000453248.6:c.307+37C>T ENSP00000391521.2:n.307+37C>T
ENST00000502594.5:c.385+37C>T ENSP00000423319.1:n.385+37C>T
ENST00000507429.5:c.*23C>T ENSP00000421470.1:n.*23C>T
ENST00000512023.5:c.235+37C>T ENSP00000424505.1:n.235+37C>T
ENST00000512506.5:c.235+37C>T ENSP00000423711.1:n.235+37C>T
ENST00000513887.5:c.157+37C>T ENSP00000422265.1:n.157+37C>T
ENST00000515813.1:n.531C>T
ENST00000631654.1:c.385+37C>T ENSP00000487839.1:n.385+37C>T
NM_001104647.1:c.385+37C>T NP_001098117.1:n.385+37C>T
NM_018155.2:c.385+37C>T NP_060625.2:n.385+37C>T
XM_006713685.2:c.-722+37C>T XP_006713748.1:n.-722+37C>T
XM_011512951.1:c.481+37C>T XP_011511253.1:n.481+37C>T
XM_011512952.1:c.-70+37C>T XP_011511254.1:n.-70+37C>T
XM_011512953.1:c.481+37C>T XP_011511255.1:n.481+37C>T
XR_924150.1:n.674+37C>T
XR_924151.1:n.674+37C>T
XR_924152.1:n.674+37C>T
XR_924153.1:n.674+37C>T
XR_924154.1:n.674+37C>T
XR_924155.1:n.674+37C>T
XR_924156.1:n.674+37C>T
XR_924157.1:n.674+37C>T
NM_001104647.3:c.385+37C>T MANE Select NP_001098117.1:n.385+37C>T
NM_018155.3:c.385+37C>T NP_060625.2:n.385+37C>T