Canonical Allele Identifier: CA64849689

Gene: ATIC

Linked Data

• dbSNP Id: rs771443605
• gnomAD v2: 2-216189977-A-G
• gnomAD v4: 2-215325254-A-G
• MyVariant Identifiers: chr2:g.216189977A>G (hg19) ; chr2:g.215325254A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215325254A>G , CM000664.2:g.215325254A>G	GRCh38
NC_000002.11:g.216189977A>G , CM000664.1:g.216189977A>G	GRCh37
NC_000002.10:g.215898222A>G	NCBI36
NG_013002.1:g.18299A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.304A>G MANE Select	ENSP00000236959.9:p.Asn102Asp
ENST00000236959.13:c.304A>G	ENSP00000236959.9:p.Asn102Asp
ENST00000413174.1:c.127A>G	ENSP00000402393.1:p.Asn43Asp
ENST00000427397.5:c.*354A>G	ENSP00000394317.1:n.*354A>G
ENST00000435675.5:c.301A>G	ENSP00000415935.1:p.Asn101Asp
ENST00000443953.5:c.*401A>G	ENSP00000406792.1:n.*401A>G
ENST00000444305.5:c.237A>G	ENSP00000388675.1:p.Ala79=
ENST00000488712.5:n.516A>G
NM_004044.6:c.304A>G	NP_004035.2:p.Asn102Asp
XM_017004187.2:c.304A>G	XP_016859676.1:p.Asn102Asp
XM_024452919.1:c.127A>G	XP_024308687.1:p.Asn43Asp
NM_004044.7:c.304A>G MANE Select	NP_004035.2:p.Asn102Asp