Canonical Allele Identifier: CA1327331602

Gene: ATIC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344579G= , CM000664.2:g.215344579G=	GRCh38
NC_000002.11:g.216209302G= , CM000664.1:g.216209302G=	GRCh37
NC_000002.10:g.215917547G=	NCBI36
NG_013002.1:g.37624G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.1228-200G= MANE Select	ENSP00000236959.9:n.1228-200G=
ENST00000236959.13:c.1228-200G=	ENSP00000236959.9:n.1228-200G=
ENST00000426233.1:c.233-200G=
ENST00000435675.5:c.1225-200G=	ENSP00000415935.1:n.1225-200G=
ENST00000443953.5:c.*1325-200G=	ENSP00000406792.1:n.*1325-200G=
ENST00000446622.5:n.308-200G=
ENST00000459796.1:n.39-200G=
ENST00000467388.1:n.140-200G=
ENST00000479093.5:n.143-200G=
NM_004044.6:c.1228-200G=	NP_004035.2:n.1228-200G=
XM_017004187.2:c.1228-200G=	XP_016859676.1:n.1228-200G=
XM_024452919.1:c.1051-200G=	XP_024308687.1:n.1051-200G=
NM_004044.7:c.1228-200G= MANE Select	NP_004035.2:n.1228-200G=