Canonical Allele Identifier: CA354858067
Gene: SLC25A36 HGNC NCBI

Linked Data

dbSNP Id: rs2107802438

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.140963182G>C , CM000665.2:g.140963182G>C GRCh38
NC_000003.11:g.140682024G>C , CM000665.1:g.140682024G>C GRCh37
NC_000003.10:g.142164714G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000324194.12:c.340G>C MANE Select ENSP00000320688.6:p.Asp114His
ENST00000648615.1:c.340G>C ENSP00000497436.1:p.Asp114His
ENST00000324194.10:c.340G>C ENSP00000320688.6:p.Asp114His
ENST00000393015.8:n.542G>C
ENST00000446041.6:c.340G>C ENSP00000401938.2:p.Asp114His
ENST00000453248.6:c.262G>C ENSP00000391521.2:p.Asp88His
ENST00000502594.5:c.340G>C ENSP00000423319.1:p.Asp114His
ENST00000507429.5:c.340G>C ENSP00000421470.1:p.Asp114His
ENST00000512023.5:c.190G>C ENSP00000424505.1:p.Asp64His
ENST00000512506.5:c.190G>C ENSP00000423711.1:p.Asp64His
ENST00000513887.5:c.112G>C ENSP00000422265.1:p.Asp38His
ENST00000515813.1:n.449G>C
ENST00000631654.1:c.340G>C ENSP00000487839.1:p.Asp114His
NM_001104647.1:c.340G>C NP_001098117.1:p.Asp114His
NM_018155.2:c.340G>C NP_060625.2:p.Asp114His
XM_006713685.2:c.-767G>C XP_006713748.1:n.-767G>C
XM_011512951.1:c.436G>C XP_011511253.1:p.Asp146His
XM_011512952.1:c.-115G>C XP_011511254.1:n.-115G>C
XM_011512953.1:c.436G>C XP_011511255.1:p.Asp146His
XR_924150.1:n.629G>C
XR_924151.1:n.629G>C
XR_924152.1:n.629G>C
XR_924153.1:n.629G>C
XR_924154.1:n.629G>C
XR_924155.1:n.629G>C
XR_924156.1:n.629G>C
XR_924157.1:n.629G>C
NM_001104647.3:c.340G>C MANE Select NP_001098117.1:p.Asp114His
NM_018155.3:c.340G>C NP_060625.2:p.Asp114His