Canonical Allele Identifier: CA1327322120
Gene: ATIC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215325323G= , CM000664.2:g.215325323G= GRCh38
NC_000002.11:g.216190046G= , CM000664.1:g.216190046G= GRCh37
NC_000002.10:g.215898291G= NCBI36
NG_013002.1:g.18368G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000236959.14:c.373G= MANE Select ENSP00000236959.9:p.Asp125=
ENST00000236959.13:c.373G= ENSP00000236959.9:p.Asp125=
ENST00000413174.1:c.196G= ENSP00000402393.1:p.Asp66=
ENST00000427397.5:c.*423G= ENSP00000394317.1:n.*423G=
ENST00000435675.5:c.370G= ENSP00000415935.1:p.Asp124=
ENST00000443953.5:c.*470G= ENSP00000406792.1:n.*470G=
ENST00000444305.5:c.*51G= ENSP00000388675.1:n.*51G=
ENST00000488712.5:n.585G=
NM_004044.6:c.373G= NP_004035.2:p.Asp125=
XM_017004187.2:c.373G= XP_016859676.1:p.Asp125=
XM_024452919.1:c.196G= XP_024308687.1:p.Asp66=
NM_004044.7:c.373G= MANE Select NP_004035.2:p.Asp125=