Canonical Allele Identifier: CA396873518
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81357912C>A , CM000678.2:g.81357912C>A GRCh38
NC_000016.9:g.81391517C>A , CM000678.1:g.81391517C>A GRCh37
NC_000016.8:g.79949018C>A NCBI36
NG_009007.1:g.47947C>A , LRG_242:g.47947C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*662C>A ENSP00000498114.1:n.*662C>A
ENST00000648994.2:c.954C>A MANE Select ENSP00000497351.1:p.Asn318Lys
ENST00000650388.1:c.488C>A ENSP00000498081.1:n.488C>A
ENST00000568107.2:c.954C>A ENSP00000476795.1:p.Asn318Lys
NM_022041.3:c.954C>A , LRG_242t1:c.954C>A NP_071324.1:p.Asn318Lys
XM_017023734.1:c.315C>A XP_016879223.1:p.Asn105Lys
NM_001377486.1:c.315C>A NP_001364415.1:p.Asn105Lys
NM_022041.4:c.954C>A MANE Select NP_071324.1:p.Asn318Lys