Canonical Allele Identifier: CA1327322106

Gene: ATIC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215325297C= , CM000664.2:g.215325297C=	GRCh38
NC_000002.11:g.216190020C= , CM000664.1:g.216190020C=	GRCh37
NC_000002.10:g.215898265C=	NCBI36
NG_013002.1:g.18342C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004044.7:c.347C= MANE Select	NP_004035.2:p.Thr116=
ENST00000236959.14:c.347C= MANE Select	ENSP00000236959.9:p.Thr116=
NM_004044.6:c.347C=	NP_004035.2:p.Thr116=
ENST00000236959.13:c.347C=	ENSP00000236959.9:p.Thr116=
ENST00000413174.1:c.170C=	ENSP00000402393.1:p.Thr57=
ENST00000427397.5:c.*397C=	ENSP00000394317.1:n.*397C=
ENST00000435675.5:c.344C=	ENSP00000415935.1:p.Thr115=
ENST00000443953.5:c.*444C=	ENSP00000406792.1:n.*444C=
ENST00000444305.5:c.*25C=	ENSP00000388675.1:n.*25C=
ENST00000488712.5:n.559C=
XM_017004187.2:c.347C=	XP_016859676.1:p.Thr116=
XM_024452919.1:c.170C=	XP_024308687.1:p.Thr57=