Canonical Allele Identifier: CA64816824

Gene: ATIC

Linked Data

• dbSNP Id: rs934717762
• MyVariant Identifiers: chr2:g.216209558T>C (hg19) ; chr2:g.215344835T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344835T>C , CM000664.2:g.215344835T>C	GRCh38
NC_000002.11:g.216209558T>C , CM000664.1:g.216209558T>C	GRCh37
NC_000002.10:g.215917803T>C	NCBI36
NG_013002.1:g.37880T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000236959.14:c.1284T>C MANE Select	ENSP00000236959.9:p.Thr428=
ENST00000236959.13:c.1284T>C	ENSP00000236959.9:p.Thr428=
ENST00000426233.1:c.289T>C
ENST00000435675.5:c.1281T>C	ENSP00000415935.1:p.Thr427=
ENST00000443953.5:c.*1381T>C	ENSP00000406792.1:n.*1381T>C
ENST00000446622.5:n.364T>C
ENST00000459796.1:n.95T>C
ENST00000467388.1:n.196T>C
ENST00000479093.5:n.199T>C
NM_004044.6:c.1284T>C	NP_004035.2:p.Thr428=
XM_017004187.2:c.1284T>C	XP_016859676.1:p.Thr428=
XM_024452919.1:c.1107T>C	XP_024308687.1:p.Thr369=
NM_004044.7:c.1284T>C MANE Select	NP_004035.2:p.Thr428=