Canonical Allele Identifier: CA396873509
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81357908T>C , CM000678.2:g.81357908T>C GRCh38
NC_000016.9:g.81391513T>C , CM000678.1:g.81391513T>C GRCh37
NC_000016.8:g.79949014T>C NCBI36
NG_009007.1:g.47943T>C , LRG_242:g.47943T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*658T>C ENSP00000498114.1:n.*658T>C
ENST00000648994.2:c.950T>C MANE Select ENSP00000497351.1:p.Ile317Thr
ENST00000650388.1:c.484T>C ENSP00000498081.1:n.484T>C
ENST00000568107.2:c.950T>C ENSP00000476795.1:p.Ile317Thr
NM_022041.3:c.950T>C , LRG_242t1:c.950T>C NP_071324.1:p.Ile317Thr
XM_017023734.1:c.311T>C XP_016879223.1:p.Ile104Thr
NM_001377486.1:c.311T>C NP_001364415.1:p.Ile104Thr
NM_022041.4:c.950T>C MANE Select NP_071324.1:p.Ile317Thr