Canonical Allele Identifier: CA8191387
Gene: GAN HGNC NCBI

Linked Data

ClinVar Variation Id: 1102381
ClinVar RCV Id: RCV001425678
dbSNP Id: rs112693832
ExAC: 16:81388255 A / G
gnomAD v2: 16-81388255-A-G
gnomAD v3: 16-81354650-A-G
gnomAD v4: 16-81354650-A-G
MyVariant Identifiers: chr16:g.81388255A>G (hg19) chr16:g.81354650A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354650A>G , CM000678.2:g.81354650A>G GRCh38
NC_000016.9:g.81388255A>G , CM000678.1:g.81388255A>G GRCh37
NC_000016.8:g.79945756A>G NCBI36
NG_009007.1:g.44685A>G , LRG_242:g.44685A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.*236A>G ENSP00000498114.1:n.*236A>G
ENST00000648994.2:c.528A>G MANE Select ENSP00000497351.1:p.Gln176=
ENST00000650388.1:c.168-2135A>G ENSP00000498081.1:n.168-2135A>G
ENST00000674788.1:n.653A>G
ENST00000568107.2:c.528A>G ENSP00000476795.1:p.Gln176=
NM_022041.3:c.528A>G , LRG_242t1:c.528A>G NP_071324.1:p.Gln176=
XM_017023734.1:c.-112A>G XP_016879223.1:n.-112A>G
NM_001377486.1:c.-112A>G NP_001364415.1:n.-112A>G
NM_022041.4:c.528A>G MANE Select NP_071324.1:p.Gln176=
Search 100 bp 5'
Search 100 bp 3'