Canonical Allele Identifier: CA1327331956
Gene: ATIC HGNC NCBI

Linked Data

dbSNP Id: rs957480
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215345437C>A , CM000664.2:g.215345437C>A GRCh38
NC_000002.11:g.216210160C>A , CM000664.1:g.216210160C>A GRCh37
NC_000002.10:g.215918405C>A NCBI36
NG_013002.1:g.38482C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000236959.14:c.1320+566C>A MANE Select ENSP00000236959.9:n.1320+566C>A
ENST00000236959.13:c.1320+566C>A ENSP00000236959.9:n.1320+566C>A
ENST00000426233.1:c.325+566C>A
ENST00000435675.5:c.1317+566C>A ENSP00000415935.1:n.1317+566C>A
ENST00000443953.5:c.*1417+566C>A ENSP00000406792.1:n.*1417+566C>A
ENST00000446622.5:n.400+566C>A
ENST00000459796.1:n.697C>A
ENST00000467388.1:n.232+566C>A
ENST00000479093.5:n.235+566C>A
NM_004044.6:c.1320+566C>A NP_004035.2:n.1320+566C>A
XM_017004187.2:c.1320+566C>A XP_016859676.1:n.1320+566C>A
XM_024452919.1:c.1143+566C>A XP_024308687.1:n.1143+566C>A
NM_004044.7:c.1320+566C>A MANE Select NP_004035.2:n.1320+566C>A
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