Canonical Allele Identifier: CA1327331721

Gene: ATIC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344838G= , CM000664.2:g.215344838G=	GRCh38
NC_000002.11:g.216209561G= , CM000664.1:g.216209561G=	GRCh37
NC_000002.10:g.215917806G=	NCBI36
NG_013002.1:g.37883G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000236959.14:c.1287G= MANE Select	ENSP00000236959.9:p.Gln429=
ENST00000236959.13:c.1287G=	ENSP00000236959.9:p.Gln429=
ENST00000426233.1:c.292G=
ENST00000435675.5:c.1284G=	ENSP00000415935.1:p.Gln428=
ENST00000443953.5:c.*1384G=	ENSP00000406792.1:n.*1384G=
ENST00000446622.5:n.367G=
ENST00000459796.1:n.98G=
ENST00000467388.1:n.199G=
ENST00000479093.5:n.202G=
NM_004044.6:c.1287G=	NP_004035.2:p.Gln429=
XM_017004187.2:c.1287G=	XP_016859676.1:p.Gln429=
XM_024452919.1:c.1110G=	XP_024308687.1:p.Gln370=
NM_004044.7:c.1287G= MANE Select	NP_004035.2:p.Gln429=