Canonical Allele Identifier: CA496698872
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354461dup , CM000678.2:g.81354461dup GRCh38
NC_000016.9:g.81388066dup , CM000678.1:g.81388066dup GRCh37
NC_000016.8:g.79945567dup NCBI36
NG_009007.1:g.44496dup , LRG_242:g.44496dup

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*47dup ENSP00000498114.1:n.*47dup
ENST00000648994.2:c.339dup MANE Select ENSP00000497351.1:p.Leu114ThrfsTer5
ENST00000650388.1:c.168-2324dup ENSP00000498081.1:n.168-2324dup
ENST00000674788.1:n.464dup
ENST00000568107.2:c.339dup ENSP00000476795.1:p.Leu114ThrfsTer5
NM_022041.3:c.339dup , LRG_242t1:c.339dup NP_071324.1:p.Leu114ThrfsTer5
XM_017023734.1:c.-301dup XP_016879223.1:n.-301dup
NM_001377486.1:c.-301dup NP_001364415.1:n.-301dup
NM_022041.4:c.339dup MANE Select NP_071324.1:p.Leu114ThrfsTer5