Canonical Allele Identifier: CA496698871
Gene: GAN HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.81388064C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354459C>T , CM000678.2:g.81354459C>T GRCh38
NC_000016.9:g.81388064C>T , CM000678.1:g.81388064C>T GRCh37
NC_000016.8:g.79945565C>T NCBI36
NG_009007.1:g.44494C>T , LRG_242:g.44494C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*45C>T ENSP00000498114.1:n.*45C>T
ENST00000648994.2:c.337C>T MANE Select ENSP00000497351.1:p.Leu113=
ENST00000650388.1:c.168-2326C>T ENSP00000498081.1:n.168-2326C>T
ENST00000674788.1:n.462C>T
ENST00000568107.2:c.337C>T ENSP00000476795.1:p.Leu113=
NM_022041.3:c.337C>T , LRG_242t1:c.337C>T NP_071324.1:p.Leu113=
XM_017023734.1:c.-303C>T XP_016879223.1:n.-303C>T
NM_001377486.1:c.-303C>T NP_001364415.1:n.-303C>T
NM_022041.4:c.337C>T MANE Select NP_071324.1:p.Leu113=