Canonical Allele Identifier: CA1327331570
Gene: ATIC HGNC NCBI

Linked Data

dbSNP Id: rs2053051683

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215344522C>G , CM000664.2:g.215344522C>G GRCh38
NC_000002.11:g.216209245C>G , CM000664.1:g.216209245C>G GRCh37
NC_000002.10:g.215917490C>G NCBI36
NG_013002.1:g.37567C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000236959.14:c.1228-257C>G MANE Select ENSP00000236959.9:n.1228-257C>G
ENST00000236959.13:c.1228-257C>G ENSP00000236959.9:n.1228-257C>G
ENST00000426233.1:c.233-257C>G
ENST00000435675.5:c.1225-257C>G ENSP00000415935.1:n.1225-257C>G
ENST00000443953.5:c.*1325-257C>G ENSP00000406792.1:n.*1325-257C>G
ENST00000446622.5:n.308-257C>G
ENST00000459796.1:n.39-257C>G
ENST00000467388.1:n.140-257C>G
ENST00000479093.5:n.143-257C>G
NM_004044.6:c.1228-257C>G NP_004035.2:n.1228-257C>G
XM_017004187.2:c.1228-257C>G XP_016859676.1:n.1228-257C>G
XM_024452919.1:c.1051-257C>G XP_024308687.1:n.1051-257C>G
NM_004044.7:c.1228-257C>G MANE Select NP_004035.2:n.1228-257C>G