Canonical Allele Identifier: CA919752033
Gene: GAN HGNC NCBI

Linked Data

dbSNP Id: rs1597407273

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81365331_81365332del , CM000678.2:g.81365331_81365332del GRCh38
NC_000016.9:g.81398936_81398937del , CM000678.1:g.81398936_81398937del GRCh37
NC_000016.8:g.79956437_79956438del NCBI36
NG_009007.1:g.55366_55367del , LRG_242:g.55366_55367del

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*1082-19_*1082-18del ENSP00000498114.1:n.*1082-19_*1082-18del
ENST00000648994.2:c.1374-19_1374-18del MANE Select ENSP00000497351.1:n.1374-19_1374-18del
ENST00000650388.1:c.908-19_908-18del ENSP00000498081.1:n.908-19_908-18del
ENST00000568107.2:c.1374-19_1374-18del ENSP00000476795.1:n.1374-19_1374-18del
NM_022041.3:c.1374-19_1374-18del , LRG_242t1:c.1374-19_1374-18del NP_071324.1:n.1374-19_1374-18del
XM_017023734.1:c.735-19_735-18del XP_016879223.1:n.735-19_735-18del
NM_001377486.1:c.735-19_735-18del NP_001364415.1:n.735-19_735-18del
NM_022041.4:c.1374-19_1374-18del MANE Select NP_071324.1:n.1374-19_1374-18del