Canonical Allele Identifier: CA2237031911
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354305T= , CM000678.2:g.81354305T= GRCh38
NC_000016.9:g.81387910T= , CM000678.1:g.81387910T= GRCh37
NC_000016.8:g.79945411T= NCBI36
NG_009007.1:g.44340T= , LRG_242:g.44340T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.168-100T= ENSP00000498114.1:n.168-100T=
ENST00000648994.2:c.283-100T= MANE Select ENSP00000497351.1:n.283-100T=
ENST00000650388.1:c.168-2480T= ENSP00000498081.1:n.168-2480T=
ENST00000674788.1:n.408-100T=
ENST00000568107.2:c.283-100T= ENSP00000476795.1:n.283-100T=
NM_022041.3:c.283-100T= , LRG_242t1:c.283-100T= NP_071324.1:n.283-100T=
XM_017023734.1:c.-357-100T= XP_016879223.1:n.-357-100T=
NM_001377486.1:c.-357-100T= NP_001364415.1:n.-357-100T=
NM_022041.4:c.283-100T= MANE Select NP_071324.1:n.283-100T=