Canonical Allele Identifier: CA8191347
Gene: GAN HGNC NCBI

Linked Data

ClinVar Variation Id: 439752
ClinVar RCV Id: RCV000507610
dbSNP Id: rs771660619
ExAC: 16:81388049 G / A
gnomAD v2: 16-81388049-G-A
gnomAD v4: 16-81354444-G-A
MyVariant Identifiers: chr16:g.81388049G>A (hg19) chr16:g.81354444G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354444G>A , CM000678.2:g.81354444G>A GRCh38
NC_000016.9:g.81388049G>A , CM000678.1:g.81388049G>A GRCh37
NC_000016.8:g.79945550G>A NCBI36
NG_009007.1:g.44479G>A , LRG_242:g.44479G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*30G>A ENSP00000498114.1:n.*30G>A
ENST00000648994.2:c.322G>A MANE Select ENSP00000497351.1:p.Ala108Thr
ENST00000650388.1:c.168-2341G>A ENSP00000498081.1:n.168-2341G>A
ENST00000674788.1:n.447G>A
ENST00000568107.2:c.322G>A ENSP00000476795.1:p.Ala108Thr
NM_022041.3:c.322G>A , LRG_242t1:c.322G>A NP_071324.1:p.Ala108Thr
XM_017023734.1:c.-318G>A XP_016879223.1:n.-318G>A
NM_001377486.1:c.-318G>A NP_001364415.1:n.-318G>A
NM_022041.4:c.322G>A MANE Select NP_071324.1:p.Ala108Thr
Search 100 bp 5'
Search 100 bp 3'