Canonical Allele Identifier: CA64860240
Gene: ATIC HGNC NCBI

Linked Data

dbSNP Id: rs777074973

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215344410_215344417del , CM000664.2:g.215344410_215344417del GRCh38
NC_000002.11:g.216209133_216209140del , CM000664.1:g.216209133_216209140del GRCh37
NC_000002.10:g.215917378_215917385del NCBI36
NG_013002.1:g.37455_37462del

Transcript Alleles

HGVS Amino-acid Change
ENST00000236959.14:c.1228-369_1228-362del MANE Select ENSP00000236959.9:n.1228-369_1228-362del
ENST00000236959.13:c.1228-369_1228-362del ENSP00000236959.9:n.1228-369_1228-362del
ENST00000426233.1:c.233-369_233-362del
ENST00000435675.5:c.1225-369_1225-362del ENSP00000415935.1:n.1225-369_1225-362del
ENST00000443953.5:c.*1325-369_*1325-362del ENSP00000406792.1:n.*1325-369_*1325-362del
ENST00000446622.5:n.308-369_308-362del
ENST00000459796.1:n.39-369_39-362del
ENST00000467388.1:n.140-369_140-362del
ENST00000479093.5:n.143-369_143-362del
NM_004044.6:c.1228-369_1228-362del NP_004035.2:n.1228-369_1228-362del
XM_017004187.2:c.1228-369_1228-362del XP_016859676.1:n.1228-369_1228-362del
XM_024452919.1:c.1051-369_1051-362del XP_024308687.1:n.1051-369_1051-362del
NM_004044.7:c.1228-369_1228-362del MANE Select NP_004035.2:n.1228-369_1228-362del