Canonical Allele Identifier: CA2237016059
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315204G= , CM000678.2:g.81315204G= GRCh38
NC_000016.9:g.81348809G= , CM000678.1:g.81348809G= GRCh37
NC_000016.8:g.79906310G= NCBI36
NG_009007.1:g.5239G= , LRG_242:g.5239G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.91G= ENSP00000498114.1:p.Asp31=
ENST00000648994.2:c.91G= MANE Select ENSP00000497351.1:p.Asp31=
ENST00000650388.1:c.91G= ENSP00000498081.1:p.Asp31=
ENST00000674788.1:n.216G=
ENST00000568107.2:c.91G= ENSP00000476795.1:p.Asp31=
NM_022041.3:c.91G= , LRG_242t1:c.91G= NP_071324.1:p.Asp31=
XM_017023734.1:c.-434G= XP_016879223.1:n.-434G=
NM_001377486.1:c.-434G= NP_001364415.1:n.-434G=
NM_022041.4:c.91G= MANE Select NP_071324.1:p.Asp31=