Canonical Allele Identifier: CA539542608

Gene: ATIC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215347616T>A , CM000664.2:g.215347616T>A	GRCh38
NC_000002.11:g.216212339T>A , CM000664.1:g.216212339T>A	GRCh37
NC_000002.10:g.215920584T>A	NCBI36
NG_013002.1:g.40661T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.1503+675T>A MANE Select	ENSP00000236959.9:n.1503+675T>A
ENST00000236959.13:c.1503+675T>A	ENSP00000236959.9:n.1503+675T>A
ENST00000426233.1:c.508+675T>A
ENST00000435675.5:c.1500+675T>A	ENSP00000415935.1:n.1500+675T>A
ENST00000443953.5:c.*1600+675T>A	ENSP00000406792.1:n.*1600+675T>A
ENST00000446622.5:n.584-5T>A
ENST00000479093.5:n.418+675T>A
NM_004044.6:c.1503+675T>A	NP_004035.2:n.1503+675T>A
XM_017004187.2:c.1503+675T>A	XP_016859676.1:n.1503+675T>A
XM_024452919.1:c.1326+675T>A	XP_024308687.1:n.1326+675T>A
NM_004044.7:c.1503+675T>A MANE Select	NP_004035.2:n.1503+675T>A