Canonical Allele Identifier: CA1327331933

Gene: ATIC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215345359G= , CM000664.2:g.215345359G=	GRCh38
NC_000002.11:g.216210082G= , CM000664.1:g.216210082G=	GRCh37
NC_000002.10:g.215918327G=	NCBI36
NG_013002.1:g.38404G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000236959.14:c.1320+488G= MANE Select	ENSP00000236959.9:n.1320+488G=
ENST00000236959.13:c.1320+488G=	ENSP00000236959.9:n.1320+488G=
ENST00000426233.1:c.325+488G=
ENST00000435675.5:c.1317+488G=	ENSP00000415935.1:n.1317+488G=
ENST00000443953.5:c.*1417+488G=	ENSP00000406792.1:n.*1417+488G=
ENST00000446622.5:n.400+488G=
ENST00000459796.1:n.619G=
ENST00000467388.1:n.232+488G=
ENST00000479093.5:n.235+488G=
NM_004044.6:c.1320+488G=	NP_004035.2:n.1320+488G=
XM_017004187.2:c.1320+488G=	XP_016859676.1:n.1320+488G=
XM_024452919.1:c.1143+488G=	XP_024308687.1:n.1143+488G=
NM_004044.7:c.1320+488G= MANE Select	NP_004035.2:n.1320+488G=