Canonical Allele Identifier: CA1327322118

Gene: ATIC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215325321T= , CM000664.2:g.215325321T=	GRCh38
NC_000002.11:g.216190044T= , CM000664.1:g.216190044T=	GRCh37
NC_000002.10:g.215898289T=	NCBI36
NG_013002.1:g.18366T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.371T= MANE Select	ENSP00000236959.9:p.Ile124=
ENST00000236959.13:c.371T=	ENSP00000236959.9:p.Ile124=
ENST00000413174.1:c.194T=	ENSP00000402393.1:p.Ile65=
ENST00000427397.5:c.*421T=	ENSP00000394317.1:n.*421T=
ENST00000435675.5:c.368T=	ENSP00000415935.1:p.Ile123=
ENST00000443953.5:c.*468T=	ENSP00000406792.1:n.*468T=
ENST00000444305.5:c.*49T=	ENSP00000388675.1:n.*49T=
ENST00000488712.5:n.583T=
NM_004044.6:c.371T=	NP_004035.2:p.Ile124=
XM_017004187.2:c.371T=	XP_016859676.1:p.Ile124=
XM_024452919.1:c.194T=	XP_024308687.1:p.Ile65=
NM_004044.7:c.371T= MANE Select	NP_004035.2:p.Ile124=