Canonical Allele Identifier: CA318369
Gene: SLC25A22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.794775_794776del , CM000673.2:g.794775_794776del GRCh38
NC_000011.9:g.794775_794776del , CM000673.1:g.794775_794776del GRCh37
NC_000011.8:g.784775_784776del NCBI36
NG_023407.1:g.8496_8497del

Transcript Alleles

HGVS Amino-acid Change
ENST00000628067.3:c.146+2_146+3del
ENST00000320230.9:c.146+2_146+3del
ENST00000456706.6:c.146+2_146+3del
ENST00000481290.5:c.146+2_146+3del
ENST00000524891.5:n.362+2_362+3del
ENST00000525010.5:n.389+2_389+3del
ENST00000525644.3:n.384+2_384+3del
ENST00000526152.5:c.146+2_146+3del
ENST00000527127.5:n.333+2_333+3del
ENST00000527723.5:c.146+2_146+3del
ENST00000527734.5:c.146+2_146+3del
ENST00000528606.5:c.146+2_146+3del
ENST00000528936.5:c.146+2_146+3del
ENST00000529066.5:c.146+2_146+3del
ENST00000529351.5:c.146+2_146+3del
ENST00000530360.2:c.146+2_146+3del
ENST00000531214.5:c.146+2_146+3del
ENST00000531437.5:c.146+2_146+3del
ENST00000531514.5:c.146+2_146+3del
ENST00000531534.5:c.146+2_146+3del
ENST00000532361.5:n.361+2_361+3del
ENST00000532459.5:n.467+2_467+3del
ENST00000532484.5:c.146+2_146+3del
ENST00000533385.5:c.146+2_146+3del
ENST00000625316.2:n.504+2_504+3del
ENST00000625419.2:c.146+2_146+3del
ENST00000625752.2:c.146+2_146+3del
ENST00000627843.2:c.146+2_146+3del
ENST00000628067.2:c.146+2_146+3del
ENST00000629602.1:n.477+2_477+3del
ENST00000629634.2:c.146+2_146+3del
NM_001191060.1:c.146+2_146+3del
NM_001191061.1:c.146+2_146+3del
NM_024698.5:c.146+2_146+3del
XM_011520369.1:c.146+2_146+3del
XM_011520370.1:c.146+2_146+3del
XM_011520371.1:c.146+2_146+3del
XM_011520370.2:c.146+2_146+3del
XM_011520371.2:c.146+2_146+3del
XM_024448687.1:c.146+2_146+3del
XM_024448688.1:c.146+2_146+3del
XM_024448689.1:c.146+2_146+3del
NM_001191061.2:c.146+2_146+3del
NM_024698.6:c.146+2_146+3del
NM_001191060.2:c.146+2_146+3del