Canonical Allele Identifier: CA2807833229
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315071_81315072insAAAGAGAGC , CM000678.2:g.81315071_81315072insAAAGAGAGC GRCh38
NC_000016.9:g.81348676_81348677insAAAGAGAGC , CM000678.1:g.81348676_81348677insAAAGAGAGC GRCh37
NC_000016.8:g.79906177_79906178insAAAGAGAGC NCBI36
NG_009007.1:g.5106_5107insAAAGAGAGC , LRG_242:g.5106_5107insAAAGAGAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.-43_-42insAAAGAGAGC ENSP00000498114.1:n.-43_-42insAAAGAGAGC
ENST00000648994.2:c.-43_-42insAAAGAGAGC MANE Select ENSP00000497351.1:n.-43_-42insAAAGAGAGC
ENST00000674788.1:n.83_84insAAAGAGAGC
ENST00000568107.2:c.-43_-42insAAAGAGAGC ENSP00000476795.1:n.-43_-42insAAAGAGAGC
NM_022041.3:c.-43_-42insAAAGAGAGC , LRG_242t1:c.-43_-42insAAAGAGAGC NP_071324.1:n.-43_-42insAAAGAGAGC
XM_017023734.1:c.-567_-566insAAAGAGAGC XP_016879223.1:n.-567_-566insAAAGAGAGC
NM_001377486.1:c.-567_-566insAAAGAGAGC NP_001364415.1:n.-567_-566insAAAGAGAGC
NM_022041.4:c.-43_-42insAAAGAGAGC MANE Select NP_071324.1:n.-43_-42insAAAGAGAGC