Canonical Allele Identifier: CA2607401601
Gene: ATIC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215344739A>G , CM000664.2:g.215344739A>G GRCh38
NC_000002.11:g.216209462A>G , CM000664.1:g.216209462A>G GRCh37
NC_000002.10:g.215917707A>G NCBI36
NG_013002.1:g.37784A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000236959.14:c.1228-40A>G MANE Select ENSP00000236959.9:n.1228-40A>G
ENST00000236959.13:c.1228-40A>G ENSP00000236959.9:n.1228-40A>G
ENST00000426233.1:c.233-40A>G
ENST00000435675.5:c.1225-40A>G ENSP00000415935.1:n.1225-40A>G
ENST00000443953.5:c.*1325-40A>G ENSP00000406792.1:n.*1325-40A>G
ENST00000446622.5:n.308-40A>G
ENST00000459796.1:n.39-40A>G
ENST00000467388.1:n.140-40A>G
ENST00000479093.5:n.143-40A>G
NM_004044.6:c.1228-40A>G NP_004035.2:n.1228-40A>G
XM_017004187.2:c.1228-40A>G XP_016859676.1:n.1228-40A>G
XM_024452919.1:c.1051-40A>G XP_024308687.1:n.1051-40A>G
NM_004044.7:c.1228-40A>G MANE Select NP_004035.2:n.1228-40A>G