Canonical Allele Identifier: CA350457338

Gene: ATIC

Linked Data

• MyVariant Identifiers: chr2:g.216209574T>G (hg19) ; chr2:g.215344851T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344851T>G , CM000664.2:g.215344851T>G	GRCh38
NC_000002.11:g.216209574T>G , CM000664.1:g.216209574T>G	GRCh37
NC_000002.10:g.215917819T>G	NCBI36
NG_013002.1:g.37896T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000236959.14:c.1300T>G MANE Select	ENSP00000236959.9:p.Cys434Gly
ENST00000236959.13:c.1300T>G	ENSP00000236959.9:p.Cys434Gly
ENST00000426233.1:c.305T>G
ENST00000435675.5:c.1297T>G	ENSP00000415935.1:p.Cys433Gly
ENST00000443953.5:c.*1397T>G	ENSP00000406792.1:n.*1397T>G
ENST00000446622.5:n.380T>G
ENST00000459796.1:n.111T>G
ENST00000467388.1:n.212T>G
ENST00000479093.5:n.215T>G
NM_004044.6:c.1300T>G	NP_004035.2:p.Cys434Gly
XM_017004187.2:c.1300T>G	XP_016859676.1:p.Cys434Gly
XM_024452919.1:c.1123T>G	XP_024308687.1:p.Cys375Gly
NM_004044.7:c.1300T>G MANE Select	NP_004035.2:p.Cys434Gly