Canonical Allele Identifier: CA396873516
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81357911A>G , CM000678.2:g.81357911A>G GRCh38
NC_000016.9:g.81391516A>G , CM000678.1:g.81391516A>G GRCh37
NC_000016.8:g.79949017A>G NCBI36
NG_009007.1:g.47946A>G , LRG_242:g.47946A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*661A>G ENSP00000498114.1:n.*661A>G
ENST00000648994.2:c.953A>G MANE Select ENSP00000497351.1:p.Asn318Ser
ENST00000650388.1:c.487A>G ENSP00000498081.1:n.487A>G
ENST00000568107.2:c.953A>G ENSP00000476795.1:p.Asn318Ser
NM_022041.3:c.953A>G , LRG_242t1:c.953A>G NP_071324.1:p.Asn318Ser
XM_017023734.1:c.314A>G XP_016879223.1:p.Asn105Ser
NM_001377486.1:c.314A>G NP_001364415.1:p.Asn105Ser
NM_022041.4:c.953A>G MANE Select NP_071324.1:p.Asn318Ser