Canonical Allele Identifier: CA2577235978

Gene: ATIC

Linked Data

• dbSNP Id: rs2106039464
• gnomAD v3: 2-215344694-CA-C
• gnomAD v4: 2-215344694-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344700del , CM000664.2:g.215344700del	GRCh38
NC_000002.11:g.216209423del , CM000664.1:g.216209423del	GRCh37
NC_000002.10:g.215917668del	NCBI36
NG_013002.1:g.37745del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.1228-79del MANE Select	ENSP00000236959.9:n.1228-79del
ENST00000236959.13:c.1228-79del	ENSP00000236959.9:n.1228-79del
ENST00000426233.1:c.233-79del
ENST00000435675.5:c.1225-79del	ENSP00000415935.1:n.1225-79del
ENST00000443953.5:c.*1325-79del	ENSP00000406792.1:n.*1325-79del
ENST00000446622.5:n.308-79del
ENST00000459796.1:n.39-79del
ENST00000467388.1:n.140-79del
ENST00000479093.5:n.143-79del
NM_004044.6:c.1228-79del	NP_004035.2:n.1228-79del
XM_017004187.2:c.1228-79del	XP_016859676.1:n.1228-79del
XM_024452919.1:c.1051-79del	XP_024308687.1:n.1051-79del
NM_004044.7:c.1228-79del MANE Select	NP_004035.2:n.1228-79del