Canonical Allele Identifier: CA396873043
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81357808A>T , CM000678.2:g.81357808A>T GRCh38
NC_000016.9:g.81391413A>T , CM000678.1:g.81391413A>T GRCh37
NC_000016.8:g.79948914A>T NCBI36
NG_009007.1:g.47843A>T , LRG_242:g.47843A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*560-2A>T ENSP00000498114.1:n.*560-2A>T
ENST00000648994.2:c.852-2A>T MANE Select ENSP00000497351.1:n.852-2A>T
ENST00000650388.1:c.386-2A>T ENSP00000498081.1:n.386-2A>T
ENST00000568107.2:c.852-2A>T ENSP00000476795.1:n.852-2A>T
NM_022041.3:c.852-2A>T , LRG_242t1:c.852-2A>T NP_071324.1:n.852-2A>T
XM_017023734.1:c.213-2A>T XP_016879223.1:n.213-2A>T
NM_001377486.1:c.213-2A>T NP_001364415.1:n.213-2A>T
NM_022041.4:c.852-2A>T MANE Select NP_071324.1:n.852-2A>T