Canonical Allele Identifier: CA396891369
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81365406G>C , CM000678.2:g.81365406G>C GRCh38
NC_000016.9:g.81399011G>C , CM000678.1:g.81399011G>C GRCh37
NC_000016.8:g.79956512G>C NCBI36
NG_009007.1:g.55441G>C , LRG_242:g.55441G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*1138G>C ENSP00000498114.1:n.*1138G>C
ENST00000648994.2:c.1430G>C MANE Select ENSP00000497351.1:p.Arg477Pro
ENST00000650388.1:c.964G>C ENSP00000498081.1:n.964G>C
ENST00000568107.2:c.1430G>C ENSP00000476795.1:p.Arg477Pro
NM_022041.3:c.1430G>C , LRG_242t1:c.1430G>C NP_071324.1:p.Arg477Pro
XM_017023734.1:c.791G>C XP_016879223.1:p.Arg264Pro
NM_001377486.1:c.791G>C NP_001364415.1:p.Arg264Pro
NM_022041.4:c.1430G>C MANE Select NP_071324.1:p.Arg477Pro