Canonical Allele Identifier: CA1327322091

Gene: ATIC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215325265C= , CM000664.2:g.215325265C=	GRCh38
NC_000002.11:g.216189988C= , CM000664.1:g.216189988C=	GRCh37
NC_000002.10:g.215898233C=	NCBI36
NG_013002.1:g.18310C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.315C= MANE Select	ENSP00000236959.9:p.Pro105=
ENST00000236959.13:c.315C=	ENSP00000236959.9:p.Pro105=
ENST00000413174.1:c.138C=	ENSP00000402393.1:p.Pro46=
ENST00000427397.5:c.*365C=	ENSP00000394317.1:n.*365C=
ENST00000435675.5:c.312C=	ENSP00000415935.1:p.Pro104=
ENST00000443953.5:c.*412C=	ENSP00000406792.1:n.*412C=
ENST00000444305.5:c.248C=	ENSP00000388675.1:p.Pro83=
ENST00000488712.5:n.527C=
NM_004044.6:c.315C=	NP_004035.2:p.Pro105=
XM_017004187.2:c.315C=	XP_016859676.1:p.Pro105=
XM_024452919.1:c.138C=	XP_024308687.1:p.Pro46=
NM_004044.7:c.315C= MANE Select	NP_004035.2:p.Pro105=