Canonical Allele Identifier: CA2634487349
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315059del , CM000678.2:g.81315059del GRCh38
NC_000016.9:g.81348664del , CM000678.1:g.81348664del GRCh37
NC_000016.8:g.79906165del NCBI36
NG_009007.1:g.5094del , LRG_242:g.5094del

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.-55del ENSP00000498114.1:n.-55del
ENST00000648994.2:c.-55del MANE Select ENSP00000497351.1:n.-55del
ENST00000674788.1:n.71del
ENST00000568107.2:c.-55del ENSP00000476795.1:n.-55del
NM_022041.3:c.-55del , LRG_242t1:c.-55del NP_071324.1:n.-55del
XM_017023734.1:c.-579del XP_016879223.1:n.-579del
NM_001377486.1:c.-579del NP_001364415.1:n.-579del
NM_022041.4:c.-55del MANE Select NP_071324.1:n.-55del