Canonical Allele Identifier: CA354858196
Gene: SLC25A36 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140963212T>C , CM000665.2:g.140963212T>C GRCh38
NC_000003.11:g.140682054T>C , CM000665.1:g.140682054T>C GRCh37
NC_000003.10:g.142164744T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000324194.12:c.370T>C MANE Select ENSP00000320688.6:p.Ser124Pro
ENST00000648615.1:c.370T>C ENSP00000497436.1:p.Ser124Pro
ENST00000324194.10:c.370T>C ENSP00000320688.6:p.Ser124Pro
ENST00000393015.8:n.572T>C
ENST00000446041.6:c.370T>C ENSP00000401938.2:p.Ser124Pro
ENST00000453248.6:c.292T>C ENSP00000391521.2:p.Ser98Pro
ENST00000502594.5:c.370T>C ENSP00000423319.1:p.Ser124Pro
ENST00000507429.5:c.370T>C ENSP00000421470.1:p.Ser124Pro
ENST00000512023.5:c.220T>C ENSP00000424505.1:p.Ser74Pro
ENST00000512506.5:c.220T>C ENSP00000423711.1:p.Ser74Pro
ENST00000513887.5:c.142T>C ENSP00000422265.1:p.Ser48Pro
ENST00000515813.1:n.479T>C
ENST00000631654.1:c.370T>C ENSP00000487839.1:p.Ser124Pro
NM_001104647.1:c.370T>C NP_001098117.1:p.Ser124Pro
NM_018155.2:c.370T>C NP_060625.2:p.Ser124Pro
XM_006713685.2:c.-737T>C XP_006713748.1:n.-737T>C
XM_011512951.1:c.466T>C XP_011511253.1:p.Ser156Pro
XM_011512952.1:c.-85T>C XP_011511254.1:n.-85T>C
XM_011512953.1:c.466T>C XP_011511255.1:p.Ser156Pro
XR_924150.1:n.659T>C
XR_924151.1:n.659T>C
XR_924152.1:n.659T>C
XR_924153.1:n.659T>C
XR_924154.1:n.659T>C
XR_924155.1:n.659T>C
XR_924156.1:n.659T>C
XR_924157.1:n.659T>C
NM_001104647.3:c.370T>C MANE Select NP_001098117.1:p.Ser124Pro
NM_018155.3:c.370T>C NP_060625.2:p.Ser124Pro