Canonical Allele Identifier: CA1327331540
Gene: ATIC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215344462_215344463delinsAC , CM000664.2:g.215344462_215344463delinsAC GRCh38
NC_000002.11:g.216209185_216209186delinsAC , CM000664.1:g.216209185_216209186delinsAC GRCh37
NC_000002.10:g.215917430_215917431delinsAC NCBI36
NG_013002.1:g.37507_37508delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000236959.14:c.1228-317_1228-316delinsAC MANE Select ENSP00000236959.9:n.1228-317_1228-316delinsAC
ENST00000236959.13:c.1228-317_1228-316delinsAC ENSP00000236959.9:n.1228-317_1228-316delinsAC
ENST00000426233.1:c.233-317_233-316delinsAC
ENST00000435675.5:c.1225-317_1225-316delinsAC ENSP00000415935.1:n.1225-317_1225-316delinsAC
ENST00000443953.5:c.*1325-317_*1325-316delinsAC ENSP00000406792.1:n.*1325-317_*1325-316delinsAC
ENST00000446622.5:n.308-317_308-316delinsAC
ENST00000459796.1:n.39-317_39-316delinsAC
ENST00000467388.1:n.140-317_140-316delinsAC
ENST00000479093.5:n.143-317_143-316delinsAC
NM_004044.6:c.1228-317_1228-316delinsAC NP_004035.2:n.1228-317_1228-316delinsAC
XM_017004187.2:c.1228-317_1228-316delinsAC XP_016859676.1:n.1228-317_1228-316delinsAC
XM_024452919.1:c.1051-317_1051-316delinsAC XP_024308687.1:n.1051-317_1051-316delinsAC
NM_004044.7:c.1228-317_1228-316delinsAC MANE Select NP_004035.2:n.1228-317_1228-316delinsAC