Canonical Allele Identifier: CA396873513
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81357910A>T , CM000678.2:g.81357910A>T GRCh38
NC_000016.9:g.81391515A>T , CM000678.1:g.81391515A>T GRCh37
NC_000016.8:g.79949016A>T NCBI36
NG_009007.1:g.47945A>T , LRG_242:g.47945A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*660A>T ENSP00000498114.1:n.*660A>T
ENST00000648994.2:c.952A>T MANE Select ENSP00000497351.1:p.Asn318Tyr
ENST00000650388.1:c.486A>T ENSP00000498081.1:n.486A>T
ENST00000568107.2:c.952A>T ENSP00000476795.1:p.Asn318Tyr
NM_022041.3:c.952A>T , LRG_242t1:c.952A>T NP_071324.1:p.Asn318Tyr
XM_017023734.1:c.313A>T XP_016879223.1:p.Asn105Tyr
NM_001377486.1:c.313A>T NP_001364415.1:p.Asn105Tyr
NM_022041.4:c.952A>T MANE Select NP_071324.1:p.Asn318Tyr