Canonical Allele Identifier: CA1327331722

Gene: ATIC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344840C= , CM000664.2:g.215344840C=	GRCh38
NC_000002.11:g.216209563C= , CM000664.1:g.216209563C=	GRCh37
NC_000002.10:g.215917808C=	NCBI36
NG_013002.1:g.37885C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000236959.14:c.1289C= MANE Select	ENSP00000236959.9:p.Ser430=
ENST00000236959.13:c.1289C=	ENSP00000236959.9:p.Ser430=
ENST00000426233.1:c.294C=
ENST00000435675.5:c.1286C=	ENSP00000415935.1:p.Ser429=
ENST00000443953.5:c.*1386C=	ENSP00000406792.1:n.*1386C=
ENST00000446622.5:n.369C=
ENST00000459796.1:n.100C=
ENST00000467388.1:n.201C=
ENST00000479093.5:n.204C=
NM_004044.6:c.1289C=	NP_004035.2:p.Ser430=
XM_017004187.2:c.1289C=	XP_016859676.1:p.Ser430=
XM_024452919.1:c.1112C=	XP_024308687.1:p.Ser371=
NM_004044.7:c.1289C= MANE Select	NP_004035.2:p.Ser430=