Canonical Allele Identifier: CA2237016399
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315320_81315326delinsCCCGGAG , CM000678.2:g.81315320_81315326delinsCCCGGAG GRCh38
NC_000016.9:g.81348925_81348931delinsCCCGGAG , CM000678.1:g.81348925_81348931delinsCCCGGAG GRCh37
NC_000016.8:g.79906426_79906432delinsCCCGGAG NCBI36
NG_009007.1:g.5355_5361delinsCCCGGAG , LRG_242:g.5355_5361delinsCCCGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.167+40_167+46delinsCCCGGAG ENSP00000498114.1:n.167+40_167+46delinsCCCGGAG
ENST00000648994.2:c.167+40_167+46delinsCCCGGAG MANE Select ENSP00000497351.1:n.167+40_167+46delinsCCCGGAG
ENST00000650388.1:c.167+40_167+46delinsCCCGGAG ENSP00000498081.1:n.167+40_167+46delinsCCCGGAG
ENST00000674788.1:n.292+40_292+46delinsCCCGGAG
ENST00000568107.2:c.167+40_167+46delinsCCCGGAG ENSP00000476795.1:n.167+40_167+46delinsCCCGGAG
NM_022041.3:c.167+40_167+46delinsCCCGGAG , LRG_242t1:c.167+40_167+46delinsCCCGGAG NP_071324.1:n.167+40_167+46delinsCCCGGAG
XM_017023734.1:c.-358+40_-358+46delinsCCCGGAG XP_016879223.1:n.-358+40_-358+46delinsCCCGGAG
NM_001377486.1:c.-358+40_-358+46delinsCCCGGAG NP_001364415.1:n.-358+40_-358+46delinsCCCGGAG
NM_022041.4:c.167+40_167+46delinsCCCGGAG MANE Select NP_071324.1:n.167+40_167+46delinsCCCGGAG