Canonical Allele Identifier: CA1327331669
Gene: ATIC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215344734A= , CM000664.2:g.215344734A= GRCh38
NC_000002.11:g.216209457A= , CM000664.1:g.216209457A= GRCh37
NC_000002.10:g.215917702A= NCBI36
NG_013002.1:g.37779A=

Transcript Alleles

HGVS Amino-acid change
ENST00000236959.14:c.1228-45A= MANE Select ENSP00000236959.9:n.1228-45A=
ENST00000236959.13:c.1228-45A= ENSP00000236959.9:n.1228-45A=
ENST00000426233.1:c.233-45A=
ENST00000435675.5:c.1225-45A= ENSP00000415935.1:n.1225-45A=
ENST00000443953.5:c.*1325-45A= ENSP00000406792.1:n.*1325-45A=
ENST00000446622.5:n.308-45A=
ENST00000459796.1:n.39-45A=
ENST00000467388.1:n.140-45A=
ENST00000479093.5:n.143-45A=
NM_004044.6:c.1228-45A= NP_004035.2:n.1228-45A=
XM_017004187.2:c.1228-45A= XP_016859676.1:n.1228-45A=
XM_024452919.1:c.1051-45A= XP_024308687.1:n.1051-45A=
NM_004044.7:c.1228-45A= MANE Select NP_004035.2:n.1228-45A=