Canonical Allele Identifier: CA396867489
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354457T>A , CM000678.2:g.81354457T>A GRCh38
NC_000016.9:g.81388062T>A , CM000678.1:g.81388062T>A GRCh37
NC_000016.8:g.79945563T>A NCBI36
NG_009007.1:g.44492T>A , LRG_242:g.44492T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*43T>A ENSP00000498114.1:n.*43T>A
ENST00000648994.2:c.335T>A MANE Select ENSP00000497351.1:p.Leu112Gln
ENST00000650388.1:c.168-2328T>A ENSP00000498081.1:n.168-2328T>A
ENST00000674788.1:n.460T>A
ENST00000568107.2:c.335T>A ENSP00000476795.1:p.Leu112Gln
NM_022041.3:c.335T>A , LRG_242t1:c.335T>A NP_071324.1:p.Leu112Gln
XM_017023734.1:c.-305T>A XP_016879223.1:n.-305T>A
NM_001377486.1:c.-305T>A NP_001364415.1:n.-305T>A
NM_022041.4:c.335T>A MANE Select NP_071324.1:p.Leu112Gln