Canonical Allele Identifier: CA1327322119

Gene: ATIC

Genomic Alleles

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

Transcript Alleles

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