Canonical Allele Identifier: CA979634587
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315026_81315027insT , CM000678.2:g.81315026_81315027insT GRCh38
NC_000016.9:g.81348631_81348632insT , CM000678.1:g.81348631_81348632insT GRCh37
NC_000016.8:g.79906132_79906133insT NCBI36
NG_009007.1:g.5061_5062insT , LRG_242:g.5061_5062insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.-88_-87insT ENSP00000498114.1:n.-88_-87insT
ENST00000648994.2:c.-88_-87insT MANE Select ENSP00000497351.1:n.-88_-87insT
ENST00000674788.1:n.38_39insT
ENST00000568107.2:c.-88_-87insT ENSP00000476795.1:n.-88_-87insT
NM_022041.3:c.-88_-87insT , LRG_242t1:c.-88_-87insT NP_071324.1:n.-88_-87insT
XM_017023734.1:c.-612_-611insT XP_016879223.1:n.-612_-611insT
NM_001377486.1:c.-612_-611insT NP_001364415.1:n.-612_-611insT
NM_022041.4:c.-88_-87insT MANE Select NP_071324.1:n.-88_-87insT