Canonical Allele Identifier: CA2237031537
Gene: GAN HGNC NCBI

Linked Data

dbSNP Id: rs1910405676

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354204G>A , CM000678.2:g.81354204G>A GRCh38
NC_000016.9:g.81387809G>A , CM000678.1:g.81387809G>A GRCh37
NC_000016.8:g.79945310G>A NCBI36
NG_009007.1:g.44239G>A , LRG_242:g.44239G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.168-201G>A ENSP00000498114.1:n.168-201G>A
ENST00000648994.2:c.283-201G>A MANE Select ENSP00000497351.1:n.283-201G>A
ENST00000650388.1:c.168-2581G>A ENSP00000498081.1:n.168-2581G>A
ENST00000674788.1:n.408-201G>A
ENST00000568107.2:c.283-201G>A ENSP00000476795.1:n.283-201G>A
NM_022041.3:c.283-201G>A , LRG_242t1:c.283-201G>A NP_071324.1:n.283-201G>A
XM_017023734.1:c.-357-201G>A XP_016879223.1:n.-357-201G>A
NM_001377486.1:c.-357-201G>A NP_001364415.1:n.-357-201G>A
NM_022041.4:c.283-201G>A MANE Select NP_071324.1:n.283-201G>A