Canonical Allele Identifier: CA64860251

Gene: ATIC

Linked Data

• dbSNP Id: rs1031895962
• gnomAD v2: 2-216209185-AC-A
• gnomAD v3: 2-215344462-AC-A
• gnomAD v4: 2-215344462-AC-A
• MyVariant Identifiers: chr2:g.216209186del (hg19) ; chr2:g.215344463del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344463del , CM000664.2:g.215344463del	GRCh38
NC_000002.11:g.216209186del , CM000664.1:g.216209186del	GRCh37
NC_000002.10:g.215917431del	NCBI36
NG_013002.1:g.37508del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.1228-316del MANE Select	ENSP00000236959.9:n.1228-316del
ENST00000236959.13:c.1228-316del	ENSP00000236959.9:n.1228-316del
ENST00000426233.1:c.233-316del
ENST00000435675.5:c.1225-316del	ENSP00000415935.1:n.1225-316del
ENST00000443953.5:c.*1325-316del	ENSP00000406792.1:n.*1325-316del
ENST00000446622.5:n.308-316del
ENST00000459796.1:n.39-316del
ENST00000467388.1:n.140-316del
ENST00000479093.5:n.143-316del
NM_004044.6:c.1228-316del	NP_004035.2:n.1228-316del
XM_017004187.2:c.1228-316del	XP_016859676.1:n.1228-316del
XM_024452919.1:c.1051-316del	XP_024308687.1:n.1051-316del
NM_004044.7:c.1228-316del MANE Select	NP_004035.2:n.1228-316del