Canonical Allele Identifier: CA1327331591

Gene: ATIC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344562_215344564delinsATG , CM000664.2:g.215344562_215344564delinsATG	GRCh38
NC_000002.11:g.216209285_216209287delinsATG , CM000664.1:g.216209285_216209287delinsATG	GRCh37
NC_000002.10:g.215917530_215917532delinsATG	NCBI36
NG_013002.1:g.37607_37609delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.1228-217_1228-215delinsATG MANE Select	ENSP00000236959.9:n.1228-217_1228-215delinsATG
ENST00000236959.13:c.1228-217_1228-215delinsATG	ENSP00000236959.9:n.1228-217_1228-215delinsATG
ENST00000426233.1:c.233-217_233-215delinsATG
ENST00000435675.5:c.1225-217_1225-215delinsATG	ENSP00000415935.1:n.1225-217_1225-215delinsATG
ENST00000443953.5:c.*1325-217_*1325-215delinsATG	ENSP00000406792.1:n.*1325-217_*1325-215delinsATG
ENST00000446622.5:n.308-217_308-215delinsATG
ENST00000459796.1:n.39-217_39-215delinsATG
ENST00000467388.1:n.140-217_140-215delinsATG
ENST00000479093.5:n.143-217_143-215delinsATG
NM_004044.6:c.1228-217_1228-215delinsATG	NP_004035.2:n.1228-217_1228-215delinsATG
XM_017004187.2:c.1228-217_1228-215delinsATG	XP_016859676.1:n.1228-217_1228-215delinsATG
XM_024452919.1:c.1051-217_1051-215delinsATG	XP_024308687.1:n.1051-217_1051-215delinsATG
NM_004044.7:c.1228-217_1228-215delinsATG MANE Select	NP_004035.2:n.1228-217_1228-215delinsATG