Canonical Allele Identifier: CA2662986982

Gene: ATIC

Linked Data

• gnomAD v4: 2-215325183-GCTGTAAACCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215325185_215325194del , CM000664.2:g.215325185_215325194del	GRCh38
NC_000002.11:g.216189908_216189917del , CM000664.1:g.216189908_216189917del	GRCh37
NC_000002.10:g.215898153_215898162del	NCBI36
NG_013002.1:g.18230_18239del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.291-56_291-47del MANE Select	ENSP00000236959.9:n.291-56_291-47del
ENST00000236959.13:c.291-56_291-47del	ENSP00000236959.9:n.291-56_291-47del
ENST00000413174.1:c.114-56_114-47del	ENSP00000402393.1:n.114-56_114-47del
ENST00000427397.5:c.*341-56_*341-47del	ENSP00000394317.1:n.*341-56_*341-47del
ENST00000435675.5:c.288-56_288-47del	ENSP00000415935.1:n.288-56_288-47del
ENST00000443953.5:c.*388-56_*388-47del	ENSP00000406792.1:n.*388-56_*388-47del
ENST00000444305.5:c.224-56_224-47del	ENSP00000388675.1:n.224-56_224-47del
ENST00000488712.5:n.447_456del
NM_004044.6:c.291-56_291-47del	NP_004035.2:n.291-56_291-47del
XM_017004187.2:c.291-56_291-47del	XP_016859676.1:n.291-56_291-47del
XM_024452919.1:c.114-56_114-47del	XP_024308687.1:n.114-56_114-47del
NM_004044.7:c.291-56_291-47del MANE Select	NP_004035.2:n.291-56_291-47del