Canonical Allele Identifier: CA1327322047
Gene: ATIC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215325200_215325201delinsTG , CM000664.2:g.215325200_215325201delinsTG GRCh38
NC_000002.11:g.216189923_216189924delinsTG , CM000664.1:g.216189923_216189924delinsTG GRCh37
NC_000002.10:g.215898168_215898169delinsTG NCBI36
NG_013002.1:g.18245_18246delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000236959.14:c.291-41_291-40delinsTG MANE Select ENSP00000236959.9:n.291-41_291-40delinsTG...
ENST00000236959.13:c.291-41_291-40delinsTG ENSP00000236959.9:n.291-41_291-40delinsTG...
ENST00000413174.1:c.114-41_114-40delinsTG ENSP00000402393.1:n.114-41_114-40delinsTG...
ENST00000427397.5:c.*341-41_*341-40delinsTG ENSP00000394317.1:n.*341-41_*341-40delins...
ENST00000435675.5:c.288-41_288-40delinsTG ENSP00000415935.1:n.288-41_288-40delinsTG...
ENST00000443953.5:c.*388-41_*388-40delinsTG ENSP00000406792.1:n.*388-41_*388-40delins...
ENST00000444305.5:c.224-41_224-40delinsTG ENSP00000388675.1:n.224-41_224-40delinsTG...
ENST00000488712.5:n.462_463delinsTG
NM_004044.6:c.291-41_291-40delinsTG NP_004035.2:n.291-41_291-40delinsTG
XM_017004187.2:c.291-41_291-40delinsTG XP_016859676.1:n.291-41_291-40delinsTG
XM_024452919.1:c.114-41_114-40delinsTG XP_024308687.1:n.114-41_114-40delinsTG
NM_004044.7:c.291-41_291-40delinsTG MANE Select NP_004035.2:n.291-41_291-40delinsTG