Canonical Allele Identifier: CA2662989474

Gene: ATIC

Linked Data

• gnomAD v4: 2-215344638-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344638G>T , CM000664.2:g.215344638G>T	GRCh38
NC_000002.11:g.216209361G>T , CM000664.1:g.216209361G>T	GRCh37
NC_000002.10:g.215917606G>T	NCBI36
NG_013002.1:g.37683G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.1228-141G>T MANE Select	ENSP00000236959.9:n.1228-141G>T
ENST00000236959.13:c.1228-141G>T	ENSP00000236959.9:n.1228-141G>T
ENST00000426233.1:c.233-141G>T
ENST00000435675.5:c.1225-141G>T	ENSP00000415935.1:n.1225-141G>T
ENST00000443953.5:c.*1325-141G>T	ENSP00000406792.1:n.*1325-141G>T
ENST00000446622.5:n.308-141G>T
ENST00000459796.1:n.39-141G>T
ENST00000467388.1:n.140-141G>T
ENST00000479093.5:n.143-141G>T
NM_004044.6:c.1228-141G>T	NP_004035.2:n.1228-141G>T
XM_017004187.2:c.1228-141G>T	XP_016859676.1:n.1228-141G>T
XM_024452919.1:c.1051-141G>T	XP_024308687.1:n.1051-141G>T
NM_004044.7:c.1228-141G>T MANE Select	NP_004035.2:n.1228-141G>T