Canonical Allele Identifier: CA496698864
Gene: GAN HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.81388054T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354449T>A , CM000678.2:g.81354449T>A GRCh38
NC_000016.9:g.81388054T>A , CM000678.1:g.81388054T>A GRCh37
NC_000016.8:g.79945555T>A NCBI36
NG_009007.1:g.44484T>A , LRG_242:g.44484T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.*35T>A ENSP00000498114.1:n.*35T>A
ENST00000648994.2:c.327T>A MANE Select ENSP00000497351.1:p.Ala109=
ENST00000650388.1:c.168-2336T>A ENSP00000498081.1:n.168-2336T>A
ENST00000674788.1:n.452T>A
ENST00000568107.2:c.327T>A ENSP00000476795.1:p.Ala109=
NM_022041.3:c.327T>A , LRG_242t1:c.327T>A NP_071324.1:p.Ala109=
XM_017023734.1:c.-313T>A XP_016879223.1:n.-313T>A
NM_001377486.1:c.-313T>A NP_001364415.1:n.-313T>A
NM_022041.4:c.327T>A MANE Select NP_071324.1:p.Ala109=