Canonical Allele Identifier: CA2237006764
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81365506C= , CM000678.2:g.81365506C= GRCh38
NC_000016.9:g.81399111C= , CM000678.1:g.81399111C= GRCh37
NC_000016.8:g.79956612C= NCBI36
NG_009007.1:g.55541C= , LRG_242:g.55541C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.*1210+28C= ENSP00000498114.1:n.*1210+28C=
ENST00000648994.2:c.1502+28C= MANE Select ENSP00000497351.1:n.1502+28C=
ENST00000650388.1:c.1036+28C= ENSP00000498081.1:n.1036+28C=
ENST00000567335.1:n.60+28C=
ENST00000568107.2:c.1502+28C= ENSP00000476795.1:n.1502+28C=
NM_022041.3:c.1502+28C= , LRG_242t1:c.1502+28C= NP_071324.1:n.1502+28C=
XM_017023734.1:c.863+28C= XP_016879223.1:n.863+28C=
NM_001377486.1:c.863+28C= NP_001364415.1:n.863+28C=
NM_022041.4:c.1502+28C= MANE Select NP_071324.1:n.1502+28C=