Canonical Allele Identifier: CA2237032913
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354587A= , CM000678.2:g.81354587A= GRCh38
NC_000016.9:g.81388192A= , CM000678.1:g.81388192A= GRCh37
NC_000016.8:g.79945693A= NCBI36
NG_009007.1:g.44622A= , LRG_242:g.44622A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.*173A= ENSP00000498114.1:n.*173A=
ENST00000648994.2:c.465A= MANE Select ENSP00000497351.1:p.Glu155=
ENST00000650388.1:c.168-2198A= ENSP00000498081.1:n.168-2198A=
ENST00000674788.1:n.590A=
ENST00000568107.2:c.465A= ENSP00000476795.1:p.Glu155=
NM_022041.3:c.465A= , LRG_242t1:c.465A= NP_071324.1:p.Glu155=
XM_017023734.1:c.-175A= XP_016879223.1:n.-175A=
NM_001377486.1:c.-175A= NP_001364415.1:n.-175A=
NM_022041.4:c.465A= MANE Select NP_071324.1:p.Glu155=