Canonical Allele Identifier: CA2237016501
Gene: GAN HGNC NCBI

Linked Data

dbSNP Id: rs1908997066

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315361dup , CM000678.2:g.81315361dup GRCh38
NC_000016.9:g.81348966dup , CM000678.1:g.81348966dup GRCh37
NC_000016.8:g.79906467dup NCBI36
NG_009007.1:g.5396dup , LRG_242:g.5396dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.167+81dup ENSP00000498114.1:n.167+81dup
ENST00000648994.2:c.167+81dup MANE Select ENSP00000497351.1:n.167+81dup
ENST00000650388.1:c.167+81dup ENSP00000498081.1:n.167+81dup
ENST00000674788.1:n.292+81dup
ENST00000568107.2:c.167+81dup ENSP00000476795.1:n.167+81dup
NM_022041.3:c.167+81dup , LRG_242t1:c.167+81dup NP_071324.1:n.167+81dup
XM_017023734.1:c.-358+81dup XP_016879223.1:n.-358+81dup
NM_001377486.1:c.-358+81dup NP_001364415.1:n.-358+81dup
NM_022041.4:c.167+81dup MANE Select NP_071324.1:n.167+81dup