Canonical Allele Identifier: CA2237006613
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81365261T= , CM000678.2:g.81365261T= GRCh38
NC_000016.9:g.81398866T= , CM000678.1:g.81398866T= GRCh37
NC_000016.8:g.79956367T= NCBI36
NG_009007.1:g.55296T= , LRG_242:g.55296T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.*1082-89T= ENSP00000498114.1:n.*1082-89T=
ENST00000648994.2:c.1374-89T= MANE Select ENSP00000497351.1:n.1374-89T=
ENST00000650388.1:c.908-89T= ENSP00000498081.1:n.908-89T=
ENST00000568107.2:c.1374-89T= ENSP00000476795.1:n.1374-89T=
NM_022041.3:c.1374-89T= , LRG_242t1:c.1374-89T= NP_071324.1:n.1374-89T=
XM_017023734.1:c.735-89T= XP_016879223.1:n.735-89T=
NM_001377486.1:c.735-89T= NP_001364415.1:n.735-89T=
NM_022041.4:c.1374-89T= MANE Select NP_071324.1:n.1374-89T=