Canonical Allele Identifier: CA623739738
Gene: GAN HGNC NCBI

Linked Data

dbSNP Id: rs1188220945
gnomAD v2: 16-81348667-C-A
gnomAD v3: 16-81315062-C-A
gnomAD v4: 16-81315062-C-A
MyVariant Identifiers: chr16:g.81348667C>A (hg19) chr16:g.81315062C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315062C>A , CM000678.2:g.81315062C>A GRCh38
NC_000016.9:g.81348667C>A , CM000678.1:g.81348667C>A GRCh37
NC_000016.8:g.79906168C>A NCBI36
NG_009007.1:g.5097C>A , LRG_242:g.5097C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.-52C>A ENSP00000498114.1:n.-52C>A
ENST00000648994.2:c.-52C>A MANE Select ENSP00000497351.1:n.-52C>A
ENST00000674788.1:n.74C>A
ENST00000568107.2:c.-52C>A ENSP00000476795.1:n.-52C>A
NM_022041.3:c.-52C>A , LRG_242t1:c.-52C>A NP_071324.1:n.-52C>A
XM_017023734.1:c.-576C>A XP_016879223.1:n.-576C>A
NM_001377486.1:c.-576C>A NP_001364415.1:n.-576C>A
NM_022041.4:c.-52C>A MANE Select NP_071324.1:n.-52C>A
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