Canonical Allele Identifier: CA1327331631

Gene: ATIC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344646T= , CM000664.2:g.215344646T=	GRCh38
NC_000002.11:g.216209369T= , CM000664.1:g.216209369T=	GRCh37
NC_000002.10:g.215917614T=	NCBI36
NG_013002.1:g.37691T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.1228-133T= MANE Select	ENSP00000236959.9:n.1228-133T=
ENST00000236959.13:c.1228-133T=	ENSP00000236959.9:n.1228-133T=
ENST00000426233.1:c.233-133T=
ENST00000435675.5:c.1225-133T=	ENSP00000415935.1:n.1225-133T=
ENST00000443953.5:c.*1325-133T=	ENSP00000406792.1:n.*1325-133T=
ENST00000446622.5:n.308-133T=
ENST00000459796.1:n.39-133T=
ENST00000467388.1:n.140-133T=
ENST00000479093.5:n.143-133T=
NM_004044.6:c.1228-133T=	NP_004035.2:n.1228-133T=
XM_017004187.2:c.1228-133T=	XP_016859676.1:n.1228-133T=
XM_024452919.1:c.1051-133T=	XP_024308687.1:n.1051-133T=
NM_004044.7:c.1228-133T= MANE Select	NP_004035.2:n.1228-133T=