Canonical Allele Identifier: CA396868862
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354661A>T , CM000678.2:g.81354661A>T GRCh38
NC_000016.9:g.81388266A>T , CM000678.1:g.81388266A>T GRCh37
NC_000016.8:g.79945767A>T NCBI36
NG_009007.1:g.44696A>T , LRG_242:g.44696A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.*247A>T ENSP00000498114.1:n.*247A>T
ENST00000648994.2:c.539A>T MANE Select ENSP00000497351.1:p.Glu180Val
ENST00000650388.1:c.168-2124A>T ENSP00000498081.1:n.168-2124A>T
ENST00000674788.1:n.664A>T
ENST00000568107.2:c.539A>T ENSP00000476795.1:p.Glu180Val
NM_022041.3:c.539A>T , LRG_242t1:c.539A>T NP_071324.1:p.Glu180Val
XM_017023734.1:c.-101A>T XP_016879223.1:n.-101A>T
NM_001377486.1:c.-101A>T NP_001364415.1:n.-101A>T
NM_022041.4:c.539A>T MANE Select NP_071324.1:p.Glu180Val