Canonical Allele Identifier: CA2634487358
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315071_81315087del , CM000678.2:g.81315071_81315087del GRCh38
NC_000016.9:g.81348676_81348692del , CM000678.1:g.81348676_81348692del GRCh37
NC_000016.8:g.79906177_79906193del NCBI36
NG_009007.1:g.5106_5122del , LRG_242:g.5106_5122del

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.-43_-27del ENSP00000498114.1:n.-43_-27del
ENST00000648994.2:c.-43_-27del MANE Select ENSP00000497351.1:n.-43_-27del
ENST00000674788.1:n.83_99del
ENST00000568107.2:c.-43_-27del ENSP00000476795.1:n.-43_-27del
NM_022041.3:c.-43_-27del , LRG_242t1:c.-43_-27del NP_071324.1:n.-43_-27del
XM_017023734.1:c.-567_-551del XP_016879223.1:n.-567_-551del
NM_001377486.1:c.-567_-551del NP_001364415.1:n.-567_-551del
NM_022041.4:c.-43_-27del MANE Select NP_071324.1:n.-43_-27del