Canonical Allele Identifier: CA2634488238
Gene: GAN HGNC NCBI

Linked Data

gnomAD v4: 16-81357733-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81357733C>G , CM000678.2:g.81357733C>G GRCh38
NC_000016.9:g.81391338C>G , CM000678.1:g.81391338C>G GRCh37
NC_000016.8:g.79948839C>G NCBI36
NG_009007.1:g.47768C>G , LRG_242:g.47768C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*560-77C>G ENSP00000498114.1:n.*560-77C>G
ENST00000648994.2:c.852-77C>G MANE Select ENSP00000497351.1:n.852-77C>G
ENST00000650388.1:c.386-77C>G ENSP00000498081.1:n.386-77C>G
ENST00000568107.2:c.852-77C>G ENSP00000476795.1:n.852-77C>G
NM_022041.3:c.852-77C>G , LRG_242t1:c.852-77C>G NP_071324.1:n.852-77C>G
XM_017023734.1:c.213-77C>G XP_016879223.1:n.213-77C>G
NM_001377486.1:c.213-77C>G NP_001364415.1:n.213-77C>G
NM_022041.4:c.852-77C>G MANE Select NP_071324.1:n.852-77C>G
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