Canonical Allele Identifier: CA2740366745
Gene: ATIC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215325217G>T , CM000664.2:g.215325217G>T GRCh38
NC_000002.11:g.216189940G>T , CM000664.1:g.216189940G>T GRCh37
NC_000002.10:g.215898185G>T NCBI36
NG_013002.1:g.18262G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000236959.14:c.291-24G>T MANE Select ENSP00000236959.9:n.291-24G>T
ENST00000236959.13:c.291-24G>T ENSP00000236959.9:n.291-24G>T
ENST00000413174.1:c.114-24G>T ENSP00000402393.1:n.114-24G>T
ENST00000427397.5:c.*341-24G>T ENSP00000394317.1:n.*341-24G>T
ENST00000435675.5:c.288-24G>T ENSP00000415935.1:n.288-24G>T
ENST00000443953.5:c.*388-24G>T ENSP00000406792.1:n.*388-24G>T
ENST00000444305.5:c.224-24G>T ENSP00000388675.1:n.224-24G>T
ENST00000488712.5:n.479G>T
NM_004044.6:c.291-24G>T NP_004035.2:n.291-24G>T
XM_017004187.2:c.291-24G>T XP_016859676.1:n.291-24G>T
XM_024452919.1:c.114-24G>T XP_024308687.1:n.114-24G>T
NM_004044.7:c.291-24G>T MANE Select NP_004035.2:n.291-24G>T