Canonical Allele Identifier: CA396891414
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81365430G>T , CM000678.2:g.81365430G>T GRCh38
NC_000016.9:g.81399035G>T , CM000678.1:g.81399035G>T GRCh37
NC_000016.8:g.79956536G>T NCBI36
NG_009007.1:g.55465G>T , LRG_242:g.55465G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*1162G>T ENSP00000498114.1:n.*1162G>T
ENST00000648994.2:c.1454G>T MANE Select ENSP00000497351.1:p.Ser485Ile
ENST00000650388.1:c.988G>T ENSP00000498081.1:n.988G>T
ENST00000567335.1:n.12G>T
ENST00000568107.2:c.1454G>T ENSP00000476795.1:p.Ser485Ile
NM_022041.3:c.1454G>T , LRG_242t1:c.1454G>T NP_071324.1:p.Ser485Ile
XM_017023734.1:c.815G>T XP_016879223.1:p.Ser272Ile
NM_001377486.1:c.815G>T NP_001364415.1:p.Ser272Ile
NM_022041.4:c.1454G>T MANE Select NP_071324.1:p.Ser485Ile