Canonical Allele Identifier: CA2577235985
Gene: ATIC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215344742del , CM000664.2:g.215344742del GRCh38
NC_000002.11:g.216209465del , CM000664.1:g.216209465del GRCh37
NC_000002.10:g.215917710del NCBI36
NG_013002.1:g.37787del

Transcript Alleles

HGVS Amino-acid change
ENST00000236959.14:c.1228-37del MANE Select ENSP00000236959.9:n.1228-37del
ENST00000236959.13:c.1228-37del ENSP00000236959.9:n.1228-37del
ENST00000426233.1:c.233-37del
ENST00000435675.5:c.1225-37del ENSP00000415935.1:n.1225-37del
ENST00000443953.5:c.*1325-37del ENSP00000406792.1:n.*1325-37del
ENST00000446622.5:n.308-37del
ENST00000459796.1:n.39-37del
ENST00000467388.1:n.140-37del
ENST00000479093.5:n.143-37del
NM_004044.6:c.1228-37del NP_004035.2:n.1228-37del
XM_017004187.2:c.1228-37del XP_016859676.1:n.1228-37del
XM_024452919.1:c.1051-37del XP_024308687.1:n.1051-37del
NM_004044.7:c.1228-37del MANE Select NP_004035.2:n.1228-37del