Canonical Allele Identifier: CA496698958
Gene: GAN HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.81391514T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81357909T>A , CM000678.2:g.81357909T>A GRCh38
NC_000016.9:g.81391514T>A , CM000678.1:g.81391514T>A GRCh37
NC_000016.8:g.79949015T>A NCBI36
NG_009007.1:g.47944T>A , LRG_242:g.47944T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*659T>A ENSP00000498114.1:n.*659T>A
ENST00000648994.2:c.951T>A MANE Select ENSP00000497351.1:p.Ile317=
ENST00000650388.1:c.485T>A ENSP00000498081.1:n.485T>A
ENST00000568107.2:c.951T>A ENSP00000476795.1:p.Ile317=
NM_022041.3:c.951T>A , LRG_242t1:c.951T>A NP_071324.1:p.Ile317=
XM_017023734.1:c.312T>A XP_016879223.1:p.Ile104=
NM_001377486.1:c.312T>A NP_001364415.1:p.Ile104=
NM_022041.4:c.951T>A MANE Select NP_071324.1:p.Ile317=