Canonical Allele Identifier: CA1327331716
Gene: ATIC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215344828A= , CM000664.2:g.215344828A= GRCh38
NC_000002.11:g.216209551A= , CM000664.1:g.216209551A= GRCh37
NC_000002.10:g.215917796A= NCBI36
NG_013002.1:g.37873A=

Transcript Alleles

HGVS Amino-acid change
ENST00000236959.14:c.1277A= MANE Select ENSP00000236959.9:p.Lys426=
ENST00000236959.13:c.1277A= ENSP00000236959.9:p.Lys426=
ENST00000426233.1:c.282A=
ENST00000435675.5:c.1274A= ENSP00000415935.1:p.Lys425=
ENST00000443953.5:c.*1374A= ENSP00000406792.1:n.*1374A=
ENST00000446622.5:n.357A=
ENST00000459796.1:n.88A=
ENST00000467388.1:n.189A=
ENST00000479093.5:n.192A=
NM_004044.6:c.1277A= NP_004035.2:p.Lys426=
XM_017004187.2:c.1277A= XP_016859676.1:p.Lys426=
XM_024452919.1:c.1100A= XP_024308687.1:p.Lys367=
NM_004044.7:c.1277A= MANE Select NP_004035.2:p.Lys426=