Canonical Allele Identifier: CA396867543
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354463T>A , CM000678.2:g.81354463T>A GRCh38
NC_000016.9:g.81388068T>A , CM000678.1:g.81388068T>A GRCh37
NC_000016.8:g.79945569T>A NCBI36
NG_009007.1:g.44498T>A , LRG_242:g.44498T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*49T>A ENSP00000498114.1:n.*49T>A
ENST00000648994.2:c.341T>A MANE Select ENSP00000497351.1:p.Leu114Gln
ENST00000650388.1:c.168-2322T>A ENSP00000498081.1:n.168-2322T>A
ENST00000674788.1:n.466T>A
ENST00000568107.2:c.341T>A ENSP00000476795.1:p.Leu114Gln
NM_022041.3:c.341T>A , LRG_242t1:c.341T>A NP_071324.1:p.Leu114Gln
XM_017023734.1:c.-299T>A XP_016879223.1:n.-299T>A
NM_001377486.1:c.-299T>A NP_001364415.1:n.-299T>A
NM_022041.4:c.341T>A MANE Select NP_071324.1:p.Leu114Gln