Canonical Allele Identifier: CA2634487269
Gene: GAN HGNC NCBI

Linked Data

gnomAD v4: 16-81315022-GGGCGGGCGCGCGCGCAGGACTCGGGCCGCTCGAGGGGTCCGGCCGGACGGTGTCGGGA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315024_81315081del , CM000678.2:g.81315024_81315081del GRCh38
NC_000016.9:g.81348629_81348686del , CM000678.1:g.81348629_81348686del GRCh37
NC_000016.8:g.79906130_79906187del NCBI36
NG_009007.1:g.5059_5116del , LRG_242:g.5059_5116del

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.-90_-33del ENSP00000498114.1:n.-90_-33del
ENST00000648994.2:c.-90_-33del MANE Select ENSP00000497351.1:n.-90_-33del
ENST00000674788.1:n.36_93del
ENST00000568107.2:c.-90_-33del ENSP00000476795.1:n.-90_-33del
NM_022041.3:c.-90_-33del , LRG_242t1:c.-90_-33del NP_071324.1:n.-90_-33del
XM_017023734.1:c.-614_-557del XP_016879223.1:n.-614_-557del
NM_001377486.1:c.-614_-557del NP_001364415.1:n.-614_-557del
NM_022041.4:c.-90_-33del MANE Select NP_071324.1:n.-90_-33del
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