Canonical Allele Identifier: CA2237016605
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315403C= , CM000678.2:g.81315403C= GRCh38
NC_000016.9:g.81349008C= , CM000678.1:g.81349008C= GRCh37
NC_000016.8:g.79906509C= NCBI36
NG_009007.1:g.5438C= , LRG_242:g.5438C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.167+123C= ENSP00000498114.1:n.167+123C=
ENST00000648994.2:c.167+123C= MANE Select ENSP00000497351.1:n.167+123C=
ENST00000650388.1:c.167+123C= ENSP00000498081.1:n.167+123C=
ENST00000674788.1:n.292+123C=
ENST00000568107.2:c.167+123C= ENSP00000476795.1:n.167+123C=
NM_022041.3:c.167+123C= , LRG_242t1:c.167+123C= NP_071324.1:n.167+123C=
XM_017023734.1:c.-358+123C= XP_016879223.1:n.-358+123C=
NM_001377486.1:c.-358+123C= NP_001364415.1:n.-358+123C=
NM_022041.4:c.167+123C= MANE Select NP_071324.1:n.167+123C=