Canonical Allele Identifier: CA1327331470

Gene: ATIC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344317_215344318delinsAG , CM000664.2:g.215344317_215344318delinsAG	GRCh38
NC_000002.11:g.216209040_216209041delinsAG , CM000664.1:g.216209040_216209041delinsAG	GRCh37
NC_000002.10:g.215917285_215917286delinsAG	NCBI36
NG_013002.1:g.37362_37363delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.1228-462_1228-461delinsAG MANE Select	ENSP00000236959.9:n.1228-462_1228-461delinsAG
ENST00000236959.13:c.1228-462_1228-461delinsAG	ENSP00000236959.9:n.1228-462_1228-461delinsAG
ENST00000426233.1:c.233-462_233-461delinsAG
ENST00000435675.5:c.1225-462_1225-461delinsAG	ENSP00000415935.1:n.1225-462_1225-461delinsAG
ENST00000443953.5:c.*1325-462_*1325-461delinsAG	ENSP00000406792.1:n.*1325-462_*1325-461delinsAG
ENST00000446622.5:n.308-462_308-461delinsAG
ENST00000459796.1:n.39-462_39-461delinsAG
ENST00000467388.1:n.140-462_140-461delinsAG
ENST00000479093.5:n.143-462_143-461delinsAG
NM_004044.6:c.1228-462_1228-461delinsAG	NP_004035.2:n.1228-462_1228-461delinsAG
XM_017004187.2:c.1228-462_1228-461delinsAG	XP_016859676.1:n.1228-462_1228-461delinsAG
XM_024452919.1:c.1051-462_1051-461delinsAG	XP_024308687.1:n.1051-462_1051-461delinsAG
NM_004044.7:c.1228-462_1228-461delinsAG MANE Select	NP_004035.2:n.1228-462_1228-461delinsAG