Canonical Allele Identifier: CA378968569
Gene: SLC25A22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.792308A>T , CM000673.2:g.792308A>T GRCh38
NC_000011.9:g.792308A>T , CM000673.1:g.792308A>T GRCh37
NC_000011.8:g.782308A>T NCBI36
NG_023407.1:g.10962T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000628067.3:c.738T>A MANE Select ENSP00000486058.1:p.Cys246Ter
ENST00000320230.9:c.738T>A ENSP00000322020.5:p.Cys246Ter
ENST00000481290.5:c.813T>A ENSP00000431829.2:p.Cys271Ter
ENST00000531214.5:c.738T>A ENSP00000437236.1:p.Cys246Ter
ENST00000627843.2:c.738T>A ENSP00000486512.1:p.Cys246Ter
ENST00000628067.2:c.738T>A ENSP00000486058.1:p.Cys246Ter
NM_001191060.1:c.738T>A NP_001177989.1:p.Cys246Ter
NM_001191061.1:c.738T>A NP_001177990.1:p.Cys246Ter
NM_024698.5:c.738T>A NP_078974.1:p.Cys246Ter
XM_011520369.1:c.738T>A XP_011518671.1:p.Cys246Ter
XM_011520370.1:c.738T>A XP_011518672.1:p.Cys246Ter
XM_011520371.1:c.738T>A XP_011518673.1:p.Cys246Ter
XM_011520370.2:c.738T>A XP_011518672.1:p.Cys246Ter
XM_011520371.2:c.738T>A XP_011518673.1:p.Cys246Ter
XM_024448687.1:c.738T>A XP_024304455.1:p.Cys246Ter
XM_024448688.1:c.738T>A XP_024304456.1:p.Cys246Ter
XM_024448689.1:c.738T>A XP_024304457.1:p.Cys246Ter
NM_001191061.2:c.738T>A MANE Select NP_001177990.1:p.Cys246Ter
NM_024698.6:c.738T>A NP_078974.1:p.Cys246Ter
NM_001191060.2:c.738T>A NP_001177989.1:p.Cys246Ter