Canonical Allele Identifier: CA155227
Gene: SLC25A19 HGNC NCBI
MIF4GD-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75273595C>T , CM000679.2:g.75273595C>T GRCh38
NC_000017.10:g.73269676C>T , CM000679.1:g.73269676C>T GRCh37
NC_000017.9:g.70781271C>T NCBI36
NG_008274.1:g.20855G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000416858.7:c.819G>A (SLC25A19) MANE Select ENSP00000397818.2:p.Leu273=
ENST00000320362.7:c.819G>A (SLC25A19) ENSP00000319574.3:p.Leu273=
ENST00000375261.8:c.648G>A (SLC25A19) ENSP00000364410.4:p.Leu216=
ENST00000402418.7:c.819G>A (SLC25A19) ENSP00000385312.3:p.Leu273=
ENST00000416858.6:c.819G>A (SLC25A19) ENSP00000397818.2:p.Leu273=
ENST00000442286.6:c.819G>A (SLC25A19) ENSP00000402202.2:p.Leu273=
ENST00000580994.5:c.819G>A (SLC25A19) ENSP00000463795.1:p.Leu273=
ENST00000582822.1:c.152-307G>A (SLC25A19)
ENST00000583332.5:c.504G>A (SLC25A19) ENSP00000462214.1:p.Leu168=
NM_001126121.1:c.819G>A (SLC25A19) NP_001119593.1:p.Leu273=
NM_001126122.1:c.819G>A (SLC25A19) NP_001119594.1:p.Leu273=
NM_021734.4:c.819G>A (SLC25A19) NP_068380.3:p.Leu273=
NR_036520.1:n.2297C>T (MIF4GD-DT)
XM_005257559.2:c.819G>A (SLC25A19) XP_005257616.1:p.Leu273=
XM_005257560.1:c.819G>A (SLC25A19) XP_005257617.1:p.Leu273=
XM_005257561.2:c.819G>A (SLC25A19) XP_005257618.1:p.Leu273=
XM_005257562.1:c.819G>A (SLC25A19) XP_005257619.1:p.Leu273=
XM_006722007.1:c.819G>A (SLC25A19) XP_006722070.1:p.Leu273=
XM_011525098.1:c.504G>A (SLC25A19) XP_011523400.1:p.Leu168=
XM_005257559.4:c.819G>A (SLC25A19) XP_005257616.1:p.Leu273=
XM_005257560.2:c.819G>A (SLC25A19) XP_005257617.1:p.Leu273=
XM_005257561.4:c.819G>A (SLC25A19) XP_005257618.1:p.Leu273=
XM_005257562.2:c.819G>A (SLC25A19) XP_005257619.1:p.Leu273=
XM_006722007.2:c.819G>A (SLC25A19) XP_006722070.1:p.Leu273=
XM_017024926.2:c.819G>A (SLC25A19) XP_016880415.1:p.Leu273=
XM_017024927.2:c.516G>A (SLC25A19) XP_016880416.1:p.Leu172=
XM_017024928.2:c.504G>A (SLC25A19) XP_016880417.1:p.Leu168=
NM_001126121.2:c.819G>A (SLC25A19) MANE Select NP_001119593.1:p.Leu273=
NM_001126122.2:c.819G>A (SLC25A19) NP_001119594.1:p.Leu273=
NM_021734.5:c.819G>A (SLC25A19) NP_068380.3:p.Leu273=