Canonical Allele Identifier: CA1327331720
Gene: ATIC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215344836C= , CM000664.2:g.215344836C= GRCh38
NC_000002.11:g.216209559C= , CM000664.1:g.216209559C= GRCh37
NC_000002.10:g.215917804C= NCBI36
NG_013002.1:g.37881C=

Transcript Alleles

HGVS Amino-acid change
ENST00000236959.14:c.1285C= MANE Select ENSP00000236959.9:p.Gln429=
ENST00000236959.13:c.1285C= ENSP00000236959.9:p.Gln429=
ENST00000426233.1:c.290C=
ENST00000435675.5:c.1282C= ENSP00000415935.1:p.Gln428=
ENST00000443953.5:c.*1382C= ENSP00000406792.1:n.*1382C=
ENST00000446622.5:n.365C=
ENST00000459796.1:n.96C=
ENST00000467388.1:n.197C=
ENST00000479093.5:n.200C=
NM_004044.6:c.1285C= NP_004035.2:p.Gln429=
XM_017004187.2:c.1285C= XP_016859676.1:p.Gln429=
XM_024452919.1:c.1108C= XP_024308687.1:p.Gln370=
NM_004044.7:c.1285C= MANE Select NP_004035.2:p.Gln429=