Canonical Allele Identifier: CA2634487357
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315063_81315068del , CM000678.2:g.81315063_81315068del GRCh38
NC_000016.9:g.81348668_81348673del , CM000678.1:g.81348668_81348673del GRCh37
NC_000016.8:g.79906169_79906174del NCBI36
NG_009007.1:g.5098_5103del , LRG_242:g.5098_5103del

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.-51_-46del ENSP00000498114.1:n.-51_-46del
ENST00000648994.2:c.-51_-46del MANE Select ENSP00000497351.1:n.-51_-46del
ENST00000674788.1:n.75_80del
ENST00000568107.2:c.-51_-46del ENSP00000476795.1:n.-51_-46del
NM_022041.3:c.-51_-46del , LRG_242t1:c.-51_-46del NP_071324.1:n.-51_-46del
XM_017023734.1:c.-575_-570del XP_016879223.1:n.-575_-570del
NM_001377486.1:c.-575_-570del NP_001364415.1:n.-575_-570del
NM_022041.4:c.-51_-46del MANE Select NP_071324.1:n.-51_-46del