Canonical Allele Identifier: CA10650937

Gene: SLC25A19 MIF4GD-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75273014A>C , CM000679.2:g.75273014A>C	GRCh38
NC_000017.10:g.73269095A>C , CM000679.1:g.73269095A>C	GRCh37
NC_000017.9:g.70780690A>C	NCBI36
NG_008274.1:g.21436T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001126121.2:c.*437T>G (SLC25A19) MANE Select	NP_001119593.1:n.*437T>G
ENST00000416858.7:c.*437T>G (SLC25A19) MANE Select	ENSP00000397818.2:n.*437T>G
NM_001126121.1:c.*437T>G (SLC25A19)	NP_001119593.1:n.*437T>G
NM_001126122.1:c.*437T>G (SLC25A19)	NP_001119594.1:n.*437T>G
NM_001126122.2:c.*437T>G (SLC25A19)	NP_001119594.1:n.*437T>G
NM_021734.4:c.*437T>G (SLC25A19)	NP_068380.3:n.*437T>G
NM_021734.5:c.*437T>G (SLC25A19)	NP_068380.3:n.*437T>G
NR_036520.1:n.1716A>C (MIF4GD-DT)
ENST00000320362.7:c.*437T>G (SLC25A19)	ENSP00000319574.3:n.*437T>G
ENST00000375261.8:c.*437T>G (SLC25A19)	ENSP00000364410.4:n.*437T>G
ENST00000402418.7:c.*437T>G (SLC25A19)	ENSP00000385312.3:n.*437T>G
ENST00000416858.6:c.*437T>G (SLC25A19)	ENSP00000397818.2:n.*437T>G
ENST00000442286.6:c.*437T>G (SLC25A19)	ENSP00000402202.2:n.*437T>G
ENST00000582822.1:c.426T>G (SLC25A19)
XM_005257559.2:c.*437T>G (SLC25A19)	XP_005257616.1:n.*437T>G
XM_005257559.4:c.*437T>G (SLC25A19)	XP_005257616.1:n.*437T>G
XM_005257560.1:c.*437T>G (SLC25A19)	XP_005257617.1:n.*437T>G
XM_005257560.2:c.*437T>G (SLC25A19)	XP_005257617.1:n.*437T>G
XM_005257561.2:c.*437T>G (SLC25A19)	XP_005257618.1:n.*437T>G
XM_005257561.4:c.*437T>G (SLC25A19)	XP_005257618.1:n.*437T>G
XM_005257562.1:c.*437T>G (SLC25A19)	XP_005257619.1:n.*437T>G
XM_005257562.2:c.*437T>G (SLC25A19)	XP_005257619.1:n.*437T>G
XM_006722007.1:c.*437T>G (SLC25A19)	XP_006722070.1:n.*437T>G
XM_006722007.2:c.*437T>G (SLC25A19)	XP_006722070.1:n.*437T>G
XM_011525098.1:c.*437T>G (SLC25A19)	XP_011523400.1:n.*437T>G
XM_017024926.2:c.*437T>G (SLC25A19)	XP_016880415.1:n.*437T>G
XM_017024927.2:c.*437T>G (SLC25A19)	XP_016880416.1:n.*437T>G
XM_017024928.2:c.*437T>G (SLC25A19)	XP_016880417.1:n.*437T>G