Canonical Allele Identifier: CA2499223704
Gene: GAN HGNC NCBI

Linked Data

ClinVar Variation Id: 1125365
ClinVar RCV Id: RCV001457063
dbSNP Id: rs2150687565

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81357805del , CM000678.2:g.81357805del GRCh38
NC_000016.9:g.81391410del , CM000678.1:g.81391410del GRCh37
NC_000016.8:g.79948911del NCBI36
NG_009007.1:g.47840del , LRG_242:g.47840del

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*560-5del ENSP00000498114.1:n.*560-5del
ENST00000648994.2:c.852-5del MANE Select ENSP00000497351.1:n.852-5del
ENST00000650388.1:c.386-5del ENSP00000498081.1:n.386-5del
ENST00000568107.2:c.852-5del ENSP00000476795.1:n.852-5del
NM_022041.3:c.852-5del , LRG_242t1:c.852-5del NP_071324.1:n.852-5del
XM_017023734.1:c.213-5del XP_016879223.1:n.213-5del
NM_001377486.1:c.213-5del NP_001364415.1:n.213-5del
NM_022041.4:c.852-5del MANE Select NP_071324.1:n.852-5del