Canonical Allele Identifier: CA1327331717

Gene: ATIC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344831A= , CM000664.2:g.215344831A=	GRCh38
NC_000002.11:g.216209554A= , CM000664.1:g.216209554A=	GRCh37
NC_000002.10:g.215917799A=	NCBI36
NG_013002.1:g.37876A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000236959.14:c.1280A= MANE Select	ENSP00000236959.9:p.Tyr427=
ENST00000236959.13:c.1280A=	ENSP00000236959.9:p.Tyr427=
ENST00000426233.1:c.285A=
ENST00000435675.5:c.1277A=	ENSP00000415935.1:p.Tyr426=
ENST00000443953.5:c.*1377A=	ENSP00000406792.1:n.*1377A=
ENST00000446622.5:n.360A=
ENST00000459796.1:n.91A=
ENST00000467388.1:n.192A=
ENST00000479093.5:n.195A=
NM_004044.6:c.1280A=	NP_004035.2:p.Tyr427=
XM_017004187.2:c.1280A=	XP_016859676.1:p.Tyr427=
XM_024452919.1:c.1103A=	XP_024308687.1:p.Tyr368=
NM_004044.7:c.1280A= MANE Select	NP_004035.2:p.Tyr427=