Canonical Allele Identifier: CA396891400
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81365423C>A , CM000678.2:g.81365423C>A GRCh38
NC_000016.9:g.81399028C>A , CM000678.1:g.81399028C>A GRCh37
NC_000016.8:g.79956529C>A NCBI36
NG_009007.1:g.55458C>A , LRG_242:g.55458C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*1155C>A ENSP00000498114.1:n.*1155C>A
ENST00000648994.2:c.1447C>A MANE Select ENSP00000497351.1:p.Gln483Lys
ENST00000650388.1:c.981C>A ENSP00000498081.1:n.981C>A
ENST00000567335.1:n.5C>A
ENST00000568107.2:c.1447C>A ENSP00000476795.1:p.Gln483Lys
NM_022041.3:c.1447C>A , LRG_242t1:c.1447C>A NP_071324.1:p.Gln483Lys
XM_017023734.1:c.808C>A XP_016879223.1:p.Gln270Lys
NM_001377486.1:c.808C>A NP_001364415.1:p.Gln270Lys
NM_022041.4:c.1447C>A MANE Select NP_071324.1:p.Gln483Lys