Canonical Allele Identifier: CA396873507
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81357907A>T , CM000678.2:g.81357907A>T GRCh38
NC_000016.9:g.81391512A>T , CM000678.1:g.81391512A>T GRCh37
NC_000016.8:g.79949013A>T NCBI36
NG_009007.1:g.47942A>T , LRG_242:g.47942A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*657A>T ENSP00000498114.1:n.*657A>T
ENST00000648994.2:c.949A>T MANE Select ENSP00000497351.1:p.Ile317Phe
ENST00000650388.1:c.483A>T ENSP00000498081.1:n.483A>T
ENST00000568107.2:c.949A>T ENSP00000476795.1:p.Ile317Phe
NM_022041.3:c.949A>T , LRG_242t1:c.949A>T NP_071324.1:p.Ile317Phe
XM_017023734.1:c.310A>T XP_016879223.1:p.Ile104Phe
NM_001377486.1:c.310A>T NP_001364415.1:p.Ile104Phe
NM_022041.4:c.949A>T MANE Select NP_071324.1:p.Ile317Phe