Canonical Allele Identifier: CA350457297

Gene: ATIC

Linked Data

• MyVariant Identifiers: chr2:g.216209555C>A (hg19) ; chr2:g.215344832C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344832C>A , CM000664.2:g.215344832C>A	GRCh38
NC_000002.11:g.216209555C>A , CM000664.1:g.216209555C>A	GRCh37
NC_000002.10:g.215917800C>A	NCBI36
NG_013002.1:g.37877C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000236959.14:c.1281C>A MANE Select	ENSP00000236959.9:p.Tyr427Ter
ENST00000236959.13:c.1281C>A	ENSP00000236959.9:p.Tyr427Ter
ENST00000426233.1:c.286C>A
ENST00000435675.5:c.1278C>A	ENSP00000415935.1:p.Tyr426Ter
ENST00000443953.5:c.*1378C>A	ENSP00000406792.1:n.*1378C>A
ENST00000446622.5:n.361C>A
ENST00000459796.1:n.92C>A
ENST00000467388.1:n.193C>A
ENST00000479093.5:n.196C>A
NM_004044.6:c.1281C>A	NP_004035.2:p.Tyr427Ter
XM_017004187.2:c.1281C>A	XP_016859676.1:p.Tyr427Ter
XM_024452919.1:c.1104C>A	XP_024308687.1:p.Tyr368Ter
NM_004044.7:c.1281C>A MANE Select	NP_004035.2:p.Tyr427Ter