Canonical Allele Identifier: CA2634487513
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315307_81315310del , CM000678.2:g.81315307_81315310del GRCh38
NC_000016.9:g.81348912_81348915del , CM000678.1:g.81348912_81348915del GRCh37
NC_000016.8:g.79906413_79906416del NCBI36
NG_009007.1:g.5342_5345del , LRG_242:g.5342_5345del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.167+27_167+30del ENSP00000498114.1:n.167+27_167+30del
ENST00000648994.2:c.167+27_167+30del MANE Select ENSP00000497351.1:n.167+27_167+30del
ENST00000650388.1:c.167+27_167+30del ENSP00000498081.1:n.167+27_167+30del
ENST00000674788.1:n.292+27_292+30del
ENST00000568107.2:c.167+27_167+30del ENSP00000476795.1:n.167+27_167+30del
NM_022041.3:c.167+27_167+30del , LRG_242t1:c.167+27_167+30del NP_071324.1:n.167+27_167+30del
XM_017023734.1:c.-358+27_-358+30del XP_016879223.1:n.-358+27_-358+30del
NM_001377486.1:c.-358+27_-358+30del NP_001364415.1:n.-358+27_-358+30del
NM_022041.4:c.167+27_167+30del MANE Select NP_071324.1:n.167+27_167+30del