Canonical Allele Identifier: CA8761038

Gene: SLC25A19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75283619C>T , CM000679.2:g.75283619C>T	GRCh38
NC_000017.10:g.73279700C>T , CM000679.1:g.73279700C>T	GRCh37
NC_000017.9:g.70791295C>T	NCBI36
NG_008274.1:g.10831G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001126121.2:c.289-26G>A MANE Select	NP_001119593.1:n.289-26G>A
ENST00000416858.7:c.289-26G>A MANE Select	ENSP00000397818.2:n.289-26G>A
NM_001126121.1:c.289-26G>A	NP_001119593.1:n.289-26G>A
NM_001126122.1:c.289-26G>A	NP_001119594.1:n.289-26G>A
NM_001126122.2:c.289-26G>A	NP_001119594.1:n.289-26G>A
NM_021734.4:c.289-26G>A	NP_068380.3:n.289-26G>A
NM_021734.5:c.289-26G>A	NP_068380.3:n.289-26G>A
ENST00000320362.7:c.289-26G>A	ENSP00000319574.3:n.289-26G>A
ENST00000375261.8:c.288+2685G>A	ENSP00000364410.4:n.288+2685G>A
ENST00000402418.7:c.289-26G>A	ENSP00000385312.3:n.289-26G>A
ENST00000416858.6:c.289-26G>A	ENSP00000397818.2:n.289-26G>A
ENST00000442286.6:c.289-26G>A	ENSP00000402202.2:n.289-26G>A
ENST00000579207.5:c.289-26G>A	ENSP00000463720.1:n.289-26G>A
ENST00000580151.5:c.289-26G>A	ENSP00000462299.1:n.289-26G>A
ENST00000580273.1:c.-15-26G>A	ENSP00000463039.1:n.-15-26G>A
ENST00000580994.5:c.289-26G>A	ENSP00000463795.1:n.289-26G>A
ENST00000581988.5:c.289-26G>A	ENSP00000463428.1:n.289-26G>A
ENST00000582822.1:c.151+2781G>A
ENST00000583332.5:c.289-26G>A	ENSP00000462214.1:n.289-26G>A
XM_005257559.2:c.289-26G>A	XP_005257616.1:n.289-26G>A
XM_005257559.4:c.289-26G>A	XP_005257616.1:n.289-26G>A
XM_005257560.1:c.289-26G>A	XP_005257617.1:n.289-26G>A
XM_005257560.2:c.289-26G>A	XP_005257617.1:n.289-26G>A
XM_005257561.2:c.289-26G>A	XP_005257618.1:n.289-26G>A
XM_005257561.4:c.289-26G>A	XP_005257618.1:n.289-26G>A
XM_005257562.1:c.289-26G>A	XP_005257619.1:n.289-26G>A
XM_005257562.2:c.289-26G>A	XP_005257619.1:n.289-26G>A
XM_006722007.1:c.289-26G>A	XP_006722070.1:n.289-26G>A
XM_006722007.2:c.289-26G>A	XP_006722070.1:n.289-26G>A
XM_011525098.1:c.289-26G>A	XP_011523400.1:n.289-26G>A
XM_017024926.2:c.289-26G>A	XP_016880415.1:n.289-26G>A
XM_017024927.2:c.-15-26G>A	XP_016880416.1:n.-15-26G>A
XM_017024928.2:c.289-26G>A	XP_016880417.1:n.289-26G>A