Canonical Allele Identifier: CA2662986988

Gene: ATIC

Linked Data

• gnomAD v4: 2-215325209-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215325209T>G , CM000664.2:g.215325209T>G	GRCh38
NC_000002.11:g.216189932T>G , CM000664.1:g.216189932T>G	GRCh37
NC_000002.10:g.215898177T>G	NCBI36
NG_013002.1:g.18254T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000236959.14:c.291-32T>G MANE Select	ENSP00000236959.9:n.291-32T>G
ENST00000236959.13:c.291-32T>G	ENSP00000236959.9:n.291-32T>G
ENST00000413174.1:c.114-32T>G	ENSP00000402393.1:n.114-32T>G
ENST00000427397.5:c.*341-32T>G	ENSP00000394317.1:n.*341-32T>G
ENST00000435675.5:c.288-32T>G	ENSP00000415935.1:n.288-32T>G
ENST00000443953.5:c.*388-32T>G	ENSP00000406792.1:n.*388-32T>G
ENST00000444305.5:c.224-32T>G	ENSP00000388675.1:n.224-32T>G
ENST00000488712.5:n.471T>G
NM_004044.6:c.291-32T>G	NP_004035.2:n.291-32T>G
XM_017004187.2:c.291-32T>G	XP_016859676.1:n.291-32T>G
XM_024452919.1:c.114-32T>G	XP_024308687.1:n.114-32T>G
NM_004044.7:c.291-32T>G MANE Select	NP_004035.2:n.291-32T>G