Canonical Allele Identifier: CA2662989532

Gene: ATIC

Linked Data

• gnomAD v4: 2-215344722-TAAAGTTAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344724_215344731del , CM000664.2:g.215344724_215344731del	GRCh38
NC_000002.11:g.216209447_216209454del , CM000664.1:g.216209447_216209454del	GRCh37
NC_000002.10:g.215917692_215917699del	NCBI36
NG_013002.1:g.37769_37776del

Transcript Alleles

HGVS	Amino-acid change
ENST00000236959.14:c.1228-55_1228-48del MANE Select	ENSP00000236959.9:n.1228-55_1228-48del
ENST00000236959.13:c.1228-55_1228-48del	ENSP00000236959.9:n.1228-55_1228-48del
ENST00000426233.1:c.233-55_233-48del
ENST00000435675.5:c.1225-55_1225-48del	ENSP00000415935.1:n.1225-55_1225-48del
ENST00000443953.5:c.*1325-55_*1325-48del	ENSP00000406792.1:n.*1325-55_*1325-48del
ENST00000446622.5:n.308-55_308-48del
ENST00000459796.1:n.39-55_39-48del
ENST00000467388.1:n.140-55_140-48del
ENST00000479093.5:n.143-55_143-48del
NM_004044.6:c.1228-55_1228-48del	NP_004035.2:n.1228-55_1228-48del
XM_017004187.2:c.1228-55_1228-48del	XP_016859676.1:n.1228-55_1228-48del
XM_024452919.1:c.1051-55_1051-48del	XP_024308687.1:n.1051-55_1051-48del
NM_004044.7:c.1228-55_1228-48del MANE Select	NP_004035.2:n.1228-55_1228-48del