Canonical Allele Identifier: CA2840805855
Gene: ATIC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215325322dup , CM000664.2:g.215325322dup GRCh38
NC_000002.11:g.216190045dup , CM000664.1:g.216190045dup GRCh37
NC_000002.10:g.215898290dup NCBI36
NG_013002.1:g.18367dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000236959.14:c.372dup MANE Select ENSP00000236959.9:p.Asp125Ter
ENST00000236959.13:c.372dup ENSP00000236959.9:p.Asp125Ter
ENST00000413174.1:c.195dup ENSP00000402393.1:p.Asp66Ter
ENST00000427397.5:c.*422dup ENSP00000394317.1:n.*422dup
ENST00000435675.5:c.369dup ENSP00000415935.1:p.Asp124Ter
ENST00000443953.5:c.*469dup ENSP00000406792.1:n.*469dup
ENST00000444305.5:c.*50dup ENSP00000388675.1:n.*50dup
ENST00000488712.5:n.584dup
NM_004044.6:c.372dup NP_004035.2:p.Asp125Ter
XM_017004187.2:c.372dup XP_016859676.1:p.Asp125Ter
XM_024452919.1:c.195dup XP_024308687.1:p.Asp66Ter
NM_004044.7:c.372dup MANE Select NP_004035.2:p.Asp125Ter