Canonical Allele Identifier: CA2662989917

Gene: ATIC

Linked Data

• gnomAD v4: 2-215345439-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215345439C>T , CM000664.2:g.215345439C>T	GRCh38
NC_000002.11:g.216210162C>T , CM000664.1:g.216210162C>T	GRCh37
NC_000002.10:g.215918407C>T	NCBI36
NG_013002.1:g.38484C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000236959.14:c.1320+568C>T MANE Select	ENSP00000236959.9:n.1320+568C>T
ENST00000236959.13:c.1320+568C>T	ENSP00000236959.9:n.1320+568C>T
ENST00000426233.1:c.325+568C>T
ENST00000435675.5:c.1317+568C>T	ENSP00000415935.1:n.1317+568C>T
ENST00000443953.5:c.*1417+568C>T	ENSP00000406792.1:n.*1417+568C>T
ENST00000446622.5:n.400+568C>T
ENST00000459796.1:n.699C>T
ENST00000467388.1:n.232+568C>T
ENST00000479093.5:n.235+568C>T
NM_004044.6:c.1320+568C>T	NP_004035.2:n.1320+568C>T
XM_017004187.2:c.1320+568C>T	XP_016859676.1:n.1320+568C>T
XM_024452919.1:c.1143+568C>T	XP_024308687.1:n.1143+568C>T
NM_004044.7:c.1320+568C>T MANE Select	NP_004035.2:n.1320+568C>T