Canonical Allele Identifier: CA431153004

Gene: ATIC

Linked Data

• MyVariant Identifiers: chr2:g.216190045T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215325322T>A , CM000664.2:g.215325322T>A	GRCh38
NC_000002.11:g.216190045T>A , CM000664.1:g.216190045T>A	GRCh37
NC_000002.10:g.215898290T>A	NCBI36
NG_013002.1:g.18367T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.372T>A MANE Select	ENSP00000236959.9:p.Ile124=
ENST00000236959.13:c.372T>A	ENSP00000236959.9:p.Ile124=
ENST00000413174.1:c.195T>A	ENSP00000402393.1:p.Ile65=
ENST00000427397.5:c.*422T>A	ENSP00000394317.1:n.*422T>A
ENST00000435675.5:c.369T>A	ENSP00000415935.1:p.Ile123=
ENST00000443953.5:c.*469T>A	ENSP00000406792.1:n.*469T>A
ENST00000444305.5:c.*50T>A	ENSP00000388675.1:n.*50T>A
ENST00000488712.5:n.584T>A
NM_004044.6:c.372T>A	NP_004035.2:p.Ile124=
XM_017004187.2:c.372T>A	XP_016859676.1:p.Ile124=
XM_024452919.1:c.195T>A	XP_024308687.1:p.Ile65=
NM_004044.7:c.372T>A MANE Select	NP_004035.2:p.Ile124=