Canonical Allele Identifier: CA396873089
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81357819A>C , CM000678.2:g.81357819A>C GRCh38
NC_000016.9:g.81391424A>C , CM000678.1:g.81391424A>C GRCh37
NC_000016.8:g.79948925A>C NCBI36
NG_009007.1:g.47854A>C , LRG_242:g.47854A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*569A>C ENSP00000498114.1:n.*569A>C
ENST00000648994.2:c.861A>C MANE Select ENSP00000497351.1:p.Lys287Asn
ENST00000650388.1:c.395A>C ENSP00000498081.1:n.395A>C
ENST00000568107.2:c.861A>C ENSP00000476795.1:p.Lys287Asn
NM_022041.3:c.861A>C , LRG_242t1:c.861A>C NP_071324.1:p.Lys287Asn
XM_017023734.1:c.222A>C XP_016879223.1:p.Lys74Asn
NM_001377486.1:c.222A>C NP_001364415.1:p.Lys74Asn
NM_022041.4:c.861A>C MANE Select NP_071324.1:p.Lys287Asn