Canonical Allele Identifier: CA350473256
Gene: ATIC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215325276C>G , CM000664.2:g.215325276C>G GRCh38
NC_000002.11:g.216189999C>G , CM000664.1:g.216189999C>G GRCh37
NC_000002.10:g.215898244C>G NCBI36
NG_013002.1:g.18321C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000236959.14:c.326C>G MANE Select ENSP00000236959.9:p.Thr109Arg
ENST00000236959.13:c.326C>G ENSP00000236959.9:p.Thr109Arg
ENST00000413174.1:c.149C>G ENSP00000402393.1:p.Thr50Arg
ENST00000427397.5:c.*376C>G ENSP00000394317.1:n.*376C>G
ENST00000435675.5:c.323C>G ENSP00000415935.1:p.Thr108Arg
ENST00000443953.5:c.*423C>G ENSP00000406792.1:n.*423C>G
ENST00000444305.5:c.*4C>G ENSP00000388675.1:n.*4C>G
ENST00000488712.5:n.538C>G
NM_004044.6:c.326C>G NP_004035.2:p.Thr109Arg
XM_017004187.2:c.326C>G XP_016859676.1:p.Thr109Arg
XM_024452919.1:c.149C>G XP_024308687.1:p.Thr50Arg
NM_004044.7:c.326C>G MANE Select NP_004035.2:p.Thr109Arg