Canonical Allele Identifier: CA213203

Gene: SLC25A19 MIF4GD-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75273449A>G , CM000679.2:g.75273449A>G	GRCh38
NC_000017.10:g.73269530A>G , CM000679.1:g.73269530A>G	GRCh37
NC_000017.9:g.70781125A>G	NCBI36
NG_008274.1:g.21001T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001126121.2:c.*2T>C (SLC25A19) MANE Select	NP_001119593.1:n.*2T>C
ENST00000416858.7:c.*2T>C (SLC25A19) MANE Select	ENSP00000397818.2:n.*2T>C
NM_001126121.1:c.*2T>C (SLC25A19)	NP_001119593.1:n.*2T>C
NM_001126122.1:c.*2T>C (SLC25A19)	NP_001119594.1:n.*2T>C
NM_001126122.2:c.*2T>C (SLC25A19)	NP_001119594.1:n.*2T>C
NM_021734.4:c.*2T>C (SLC25A19)	NP_068380.3:n.*2T>C
NM_021734.5:c.*2T>C (SLC25A19)	NP_068380.3:n.*2T>C
NR_036520.1:n.2151A>G (MIF4GD-DT)
ENST00000320362.7:c.*2T>C (SLC25A19)	ENSP00000319574.3:n.*2T>C
ENST00000375261.8:c.*2T>C (SLC25A19)	ENSP00000364410.4:n.*2T>C
ENST00000402418.7:c.*2T>C (SLC25A19)	ENSP00000385312.3:n.*2T>C
ENST00000416858.6:c.*2T>C (SLC25A19)	ENSP00000397818.2:n.*2T>C
ENST00000442286.6:c.*2T>C (SLC25A19)	ENSP00000402202.2:n.*2T>C
ENST00000580994.5:c.*2T>C (SLC25A19)	ENSP00000463795.1:n.*2T>C
ENST00000582822.1:c.152-161T>C (SLC25A19)
XM_005257559.2:c.*2T>C (SLC25A19)	XP_005257616.1:n.*2T>C
XM_005257559.4:c.*2T>C (SLC25A19)	XP_005257616.1:n.*2T>C
XM_005257560.1:c.*2T>C (SLC25A19)	XP_005257617.1:n.*2T>C
XM_005257560.2:c.*2T>C (SLC25A19)	XP_005257617.1:n.*2T>C
XM_005257561.2:c.*2T>C (SLC25A19)	XP_005257618.1:n.*2T>C
XM_005257561.4:c.*2T>C (SLC25A19)	XP_005257618.1:n.*2T>C
XM_005257562.1:c.*2T>C (SLC25A19)	XP_005257619.1:n.*2T>C
XM_005257562.2:c.*2T>C (SLC25A19)	XP_005257619.1:n.*2T>C
XM_006722007.1:c.*2T>C (SLC25A19)	XP_006722070.1:n.*2T>C
XM_006722007.2:c.*2T>C (SLC25A19)	XP_006722070.1:n.*2T>C
XM_011525098.1:c.*2T>C (SLC25A19)	XP_011523400.1:n.*2T>C
XM_017024926.2:c.*2T>C (SLC25A19)	XP_016880415.1:n.*2T>C
XM_017024927.2:c.*2T>C (SLC25A19)	XP_016880416.1:n.*2T>C
XM_017024928.2:c.*2T>C (SLC25A19)	XP_016880417.1:n.*2T>C