Canonical Allele Identifier: CA396873511
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81357909T>G , CM000678.2:g.81357909T>G GRCh38
NC_000016.9:g.81391514T>G , CM000678.1:g.81391514T>G GRCh37
NC_000016.8:g.79949015T>G NCBI36
NG_009007.1:g.47944T>G , LRG_242:g.47944T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*659T>G ENSP00000498114.1:n.*659T>G
ENST00000648994.2:c.951T>G MANE Select ENSP00000497351.1:p.Ile317Met
ENST00000650388.1:c.485T>G ENSP00000498081.1:n.485T>G
ENST00000568107.2:c.951T>G ENSP00000476795.1:p.Ile317Met
NM_022041.3:c.951T>G , LRG_242t1:c.951T>G NP_071324.1:p.Ile317Met
XM_017023734.1:c.312T>G XP_016879223.1:p.Ile104Met
NM_001377486.1:c.312T>G NP_001364415.1:p.Ile104Met
NM_022041.4:c.951T>G MANE Select NP_071324.1:p.Ile317Met