Canonical Allele Identifier: CA2662986911

Gene: ATIC

Linked Data

• gnomAD v4: 2-215325105-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215325105T>A , CM000664.2:g.215325105T>A	GRCh38
NC_000002.11:g.216189828T>A , CM000664.1:g.216189828T>A	GRCh37
NC_000002.10:g.215898073T>A	NCBI36
NG_013002.1:g.18150T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.291-136T>A MANE Select	ENSP00000236959.9:n.291-136T>A
ENST00000236959.13:c.291-136T>A	ENSP00000236959.9:n.291-136T>A
ENST00000413174.1:c.114-136T>A	ENSP00000402393.1:n.114-136T>A
ENST00000427397.5:c.*341-136T>A	ENSP00000394317.1:n.*341-136T>A
ENST00000435675.5:c.288-136T>A	ENSP00000415935.1:n.288-136T>A
ENST00000443953.5:c.*388-136T>A	ENSP00000406792.1:n.*388-136T>A
ENST00000444305.5:c.224-136T>A	ENSP00000388675.1:n.224-136T>A
ENST00000488712.5:n.442-75T>A
NM_004044.6:c.291-136T>A	NP_004035.2:n.291-136T>A
XM_017004187.2:c.291-136T>A	XP_016859676.1:n.291-136T>A
XM_024452919.1:c.114-136T>A	XP_024308687.1:n.114-136T>A
NM_004044.7:c.291-136T>A MANE Select	NP_004035.2:n.291-136T>A