Canonical Allele Identifier: CA1327331469

Gene: ATIC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344316_215344319delinsTAGG , CM000664.2:g.215344316_215344319delinsTAGG	GRCh38
NC_000002.11:g.216209039_216209042delinsTAGG , CM000664.1:g.216209039_216209042delinsTAGG	GRCh37
NC_000002.10:g.215917284_215917287delinsTAGG	NCBI36
NG_013002.1:g.37361_37364delinsTAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.1228-463_1228-460delinsTAGG MANE Select	ENSP00000236959.9:n.1228-463_1228-460delinsTAGG
ENST00000236959.13:c.1228-463_1228-460delinsTAGG	ENSP00000236959.9:n.1228-463_1228-460delinsTAGG
ENST00000426233.1:c.233-463_233-460delinsTAGG
ENST00000435675.5:c.1225-463_1225-460delinsTAGG	ENSP00000415935.1:n.1225-463_1225-460delinsTAGG
ENST00000443953.5:c.*1325-463_*1325-460delinsTAGG	ENSP00000406792.1:n.*1325-463_*1325-460delinsTAGG
ENST00000446622.5:n.308-463_308-460delinsTAGG
ENST00000459796.1:n.39-463_39-460delinsTAGG
ENST00000467388.1:n.140-463_140-460delinsTAGG
ENST00000479093.5:n.143-463_143-460delinsTAGG
NM_004044.6:c.1228-463_1228-460delinsTAGG	NP_004035.2:n.1228-463_1228-460delinsTAGG
XM_017004187.2:c.1228-463_1228-460delinsTAGG	XP_016859676.1:n.1228-463_1228-460delinsTAGG
XM_024452919.1:c.1051-463_1051-460delinsTAGG	XP_024308687.1:n.1051-463_1051-460delinsTAGG
NM_004044.7:c.1228-463_1228-460delinsTAGG MANE Select	NP_004035.2:n.1228-463_1228-460delinsTAGG