Canonical Allele Identifier: CA2662989497

Gene: ATIC

Linked Data

• gnomAD v4: 2-215344665-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344666_215344667insAA , CM000664.2:g.215344666_215344667insAA	GRCh38
NC_000002.11:g.216209389_216209390insAA , CM000664.1:g.216209389_216209390insAA	GRCh37
NC_000002.10:g.215917634_215917635insAA	NCBI36
NG_013002.1:g.37711_37712insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.1228-113_1228-112insAA MANE Select	ENSP00000236959.9:n.1228-113_1228-112insAA
ENST00000236959.13:c.1228-113_1228-112insAA	ENSP00000236959.9:n.1228-113_1228-112insAA
ENST00000426233.1:c.233-113_233-112insAA
ENST00000435675.5:c.1225-113_1225-112insAA	ENSP00000415935.1:n.1225-113_1225-112insAA
ENST00000443953.5:c.*1325-113_*1325-112insAA	ENSP00000406792.1:n.*1325-113_*1325-112insAA
ENST00000446622.5:n.308-113_308-112insAA
ENST00000459796.1:n.39-113_39-112insAA
ENST00000467388.1:n.140-113_140-112insAA
ENST00000479093.5:n.143-113_143-112insAA
NM_004044.6:c.1228-113_1228-112insAA	NP_004035.2:n.1228-113_1228-112insAA
XM_017004187.2:c.1228-113_1228-112insAA	XP_016859676.1:n.1228-113_1228-112insAA
XM_024452919.1:c.1051-113_1051-112insAA	XP_024308687.1:n.1051-113_1051-112insAA
NM_004044.7:c.1228-113_1228-112insAA MANE Select	NP_004035.2:n.1228-113_1228-112insAA