Canonical Allele Identifier: CA979634620
Gene: GAN HGNC NCBI

Linked Data

dbSNP Id: rs752302389

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315063G>T , CM000678.2:g.81315063G>T GRCh38
NC_000016.9:g.81348668G>T , CM000678.1:g.81348668G>T GRCh37
NC_000016.8:g.79906169G>T NCBI36
NG_009007.1:g.5098G>T , LRG_242:g.5098G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.-51G>T ENSP00000498114.1:n.-51G>T
ENST00000648994.2:c.-51G>T MANE Select ENSP00000497351.1:n.-51G>T
ENST00000674788.1:n.75G>T
ENST00000568107.2:c.-51G>T ENSP00000476795.1:n.-51G>T
NM_022041.3:c.-51G>T , LRG_242t1:c.-51G>T NP_071324.1:n.-51G>T
XM_017023734.1:c.-575G>T XP_016879223.1:n.-575G>T
NM_001377486.1:c.-575G>T NP_001364415.1:n.-575G>T
NM_022041.4:c.-51G>T MANE Select NP_071324.1:n.-51G>T