Canonical Allele Identifier: CA1327326088
Gene: ATIC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215333248T>A , CM000664.2:g.215333248T>A GRCh38
NC_000002.11:g.216197971T>A , CM000664.1:g.216197971T>A GRCh37
NC_000002.10:g.215906216T>A NCBI36
NG_013002.1:g.26293T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000236959.14:c.815-102T>A MANE Select ENSP00000236959.9:n.815-102T>A
ENST00000236959.13:c.815-102T>A ENSP00000236959.9:n.815-102T>A
ENST00000427397.5:c.*708-102T>A ENSP00000394317.1:n.*708-102T>A
ENST00000435675.5:c.812-102T>A ENSP00000415935.1:n.812-102T>A
ENST00000443953.5:c.*912-102T>A ENSP00000406792.1:n.*912-102T>A
NM_004044.6:c.815-102T>A NP_004035.2:n.815-102T>A
XM_017004187.2:c.815-102T>A XP_016859676.1:n.815-102T>A
XM_024452919.1:c.638-102T>A XP_024308687.1:n.638-102T>A
NM_004044.7:c.815-102T>A MANE Select NP_004035.2:n.815-102T>A