Canonical Allele Identifier: CA2237032390
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354453C= , CM000678.2:g.81354453C= GRCh38
NC_000016.9:g.81388058C= , CM000678.1:g.81388058C= GRCh37
NC_000016.8:g.79945559C= NCBI36
NG_009007.1:g.44488C= , LRG_242:g.44488C=

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*39C= ENSP00000498114.1:n.*39C=
ENST00000648994.2:c.331C= MANE Select ENSP00000497351.1:p.Leu111=
ENST00000650388.1:c.168-2332C= ENSP00000498081.1:n.168-2332C=
ENST00000674788.1:n.456C=
ENST00000568107.2:c.331C= ENSP00000476795.1:p.Leu111=
NM_022041.3:c.331C= , LRG_242t1:c.331C= NP_071324.1:p.Leu111=
XM_017023734.1:c.-309C= XP_016879223.1:n.-309C=
NM_001377486.1:c.-309C= NP_001364415.1:n.-309C=
NM_022041.4:c.331C= MANE Select NP_071324.1:p.Leu111=