Canonical Allele Identifier: CA5789265

Gene: SLC25A22

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.793523C>T , CM000673.2:g.793523C>T	GRCh38
NC_000011.9:g.793523C>T , CM000673.1:g.793523C>T	GRCh37
NC_000011.8:g.783523C>T	NCBI36
NG_023407.1:g.9747G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000628067.3:c.293+6G>A MANE Select	ENSP00000486058.1:n.293+6G>A
ENST00000320230.9:c.293+6G>A	ENSP00000322020.5:n.293+6G>A
ENST00000456706.6:c.293+6G>A	ENSP00000392749.3:n.293+6G>A
ENST00000481290.5:c.368+6G>A	ENSP00000431829.2:n.368+6G>A
ENST00000524891.5:n.515G>A
ENST00000526152.5:c.293+6G>A	ENSP00000436745.1:n.293+6G>A
ENST00000527723.5:c.293+6G>A	ENSP00000434479.2:n.293+6G>A
ENST00000527734.5:c.*79+6G>A	ENSP00000433655.1:n.*79+6G>A
ENST00000528606.5:c.293+6G>A	ENSP00000437045.2:n.293+6G>A
ENST00000528936.5:c.293+6G>A	ENSP00000432817.2:n.293+6G>A
ENST00000529351.5:c.*79+6G>A	ENSP00000432222.1:n.*79+6G>A
ENST00000531214.5:c.293+6G>A	ENSP00000437236.1:n.293+6G>A
ENST00000531437.5:c.281+6G>A	ENSP00000435862.1:n.281+6G>A
ENST00000531514.5:c.*79+6G>A	ENSP00000433780.2:n.*79+6G>A
ENST00000531534.5:c.293+6G>A	ENSP00000435402.2:n.293+6G>A
ENST00000532484.5:c.293+6G>A	ENSP00000431466.2:n.293+6G>A
ENST00000533385.5:c.293+6G>A	ENSP00000434287.2:n.293+6G>A
ENST00000625419.2:c.293+6G>A	ENSP00000485719.1:n.293+6G>A
ENST00000625752.2:c.293+6G>A	ENSP00000487237.1:n.293+6G>A
ENST00000627843.2:c.293+6G>A	ENSP00000486512.1:n.293+6G>A
ENST00000628067.2:c.293+6G>A	ENSP00000486058.1:n.293+6G>A
ENST00000630809.2:n.161+6G>A
NM_001191060.1:c.293+6G>A	NP_001177989.1:n.293+6G>A
NM_001191061.1:c.293+6G>A	NP_001177990.1:n.293+6G>A
NM_024698.5:c.293+6G>A	NP_078974.1:n.293+6G>A
XM_011520369.1:c.293+6G>A	XP_011518671.1:n.293+6G>A
XM_011520370.1:c.293+6G>A	XP_011518672.1:n.293+6G>A
XM_011520371.1:c.293+6G>A	XP_011518673.1:n.293+6G>A
XM_011520370.2:c.293+6G>A	XP_011518672.1:n.293+6G>A
XM_011520371.2:c.293+6G>A	XP_011518673.1:n.293+6G>A
XM_024448687.1:c.293+6G>A	XP_024304455.1:n.293+6G>A
XM_024448688.1:c.293+6G>A	XP_024304456.1:n.293+6G>A
XM_024448689.1:c.293+6G>A	XP_024304457.1:n.293+6G>A
NM_001191061.2:c.293+6G>A MANE Select	NP_001177990.1:n.293+6G>A
NM_024698.6:c.293+6G>A	NP_078974.1:n.293+6G>A
NM_001191060.2:c.293+6G>A	NP_001177989.1:n.293+6G>A