Canonical Allele Identifier: CA2634487337
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315053_81315058del , CM000678.2:g.81315053_81315058del GRCh38
NC_000016.9:g.81348658_81348663del , CM000678.1:g.81348658_81348663del GRCh37
NC_000016.8:g.79906159_79906164del NCBI36
NG_009007.1:g.5088_5093del , LRG_242:g.5088_5093del

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.-61_-56del ENSP00000498114.1:n.-61_-56del
ENST00000648994.2:c.-61_-56del MANE Select ENSP00000497351.1:n.-61_-56del
ENST00000674788.1:n.65_70del
ENST00000568107.2:c.-61_-56del ENSP00000476795.1:n.-61_-56del
NM_022041.3:c.-61_-56del , LRG_242t1:c.-61_-56del NP_071324.1:n.-61_-56del
XM_017023734.1:c.-585_-580del XP_016879223.1:n.-585_-580del
NM_001377486.1:c.-585_-580del NP_001364415.1:n.-585_-580del
NM_022041.4:c.-61_-56del MANE Select NP_071324.1:n.-61_-56del