Canonical Allele Identifier: CA1327322058
Gene: ATIC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215325212T= , CM000664.2:g.215325212T= GRCh38
NC_000002.11:g.216189935T= , CM000664.1:g.216189935T= GRCh37
NC_000002.10:g.215898180T= NCBI36
NG_013002.1:g.18257T=

Transcript Alleles

HGVS Amino-acid change
ENST00000236959.14:c.291-29T= MANE Select ENSP00000236959.9:n.291-29T=
ENST00000236959.13:c.291-29T= ENSP00000236959.9:n.291-29T=
ENST00000413174.1:c.114-29T= ENSP00000402393.1:n.114-29T=
ENST00000427397.5:c.*341-29T= ENSP00000394317.1:n.*341-29T=
ENST00000435675.5:c.288-29T= ENSP00000415935.1:n.288-29T=
ENST00000443953.5:c.*388-29T= ENSP00000406792.1:n.*388-29T=
ENST00000444305.5:c.224-29T= ENSP00000388675.1:n.224-29T=
ENST00000488712.5:n.474T=
NM_004044.6:c.291-29T= NP_004035.2:n.291-29T=
XM_017004187.2:c.291-29T= XP_016859676.1:n.291-29T=
XM_024452919.1:c.114-29T= XP_024308687.1:n.114-29T=
NM_004044.7:c.291-29T= MANE Select NP_004035.2:n.291-29T=