Canonical Allele Identifier: CA350473445

Gene: ATIC

Linked Data

• dbSNP Id: rs2052811582
• MyVariant Identifiers: chr2:g.216190046G>A (hg19) ; chr2:g.215325323G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215325323G>A , CM000664.2:g.215325323G>A	GRCh38
NC_000002.11:g.216190046G>A , CM000664.1:g.216190046G>A	GRCh37
NC_000002.10:g.215898291G>A	NCBI36
NG_013002.1:g.18368G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.373G>A MANE Select	ENSP00000236959.9:p.Asp125Asn
ENST00000236959.13:c.373G>A	ENSP00000236959.9:p.Asp125Asn
ENST00000413174.1:c.196G>A	ENSP00000402393.1:p.Asp66Asn
ENST00000427397.5:c.*423G>A	ENSP00000394317.1:n.*423G>A
ENST00000435675.5:c.370G>A	ENSP00000415935.1:p.Asp124Asn
ENST00000443953.5:c.*470G>A	ENSP00000406792.1:n.*470G>A
ENST00000444305.5:c.*51G>A	ENSP00000388675.1:n.*51G>A
ENST00000488712.5:n.585G>A
NM_004044.6:c.373G>A	NP_004035.2:p.Asp125Asn
XM_017004187.2:c.373G>A	XP_016859676.1:p.Asp125Asn
XM_024452919.1:c.196G>A	XP_024308687.1:p.Asp66Asn
NM_004044.7:c.373G>A MANE Select	NP_004035.2:p.Asp125Asn