Canonical Allele Identifier: CA2237043080
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81358100_81358104delinsTGTCA , CM000678.2:g.81358100_81358104delinsTGTCA GRCh38
NC_000016.9:g.81391705_81391709delinsTGTCA , CM000678.1:g.81391705_81391709delinsTGTCA GRCh37
NC_000016.8:g.79949206_79949210delinsTGTCA NCBI36
NG_009007.1:g.48135_48139delinsTGTCA , LRG_242:g.48135_48139delinsTGTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.*681+169_*681+173delinsTGTCA ENSP00000498114.1:n.*681+169_*681+173delinsTGTCA
ENST00000648994.2:c.973+169_973+173delinsTGTCA MANE Select ENSP00000497351.1:n.973+169_973+173delinsTGTCA
ENST00000650388.1:c.507+169_507+173delinsTGTCA ENSP00000498081.1:n.507+169_507+173delinsTGTCA
ENST00000568107.2:c.973+169_973+173delinsTGTCA ENSP00000476795.1:n.973+169_973+173delinsTGTCA
NM_022041.3:c.973+169_973+173delinsTGTCA , LRG_242t1:c.973+169_973+173delinsTGTCA NP_071324.1:n.973+169_973+173delinsTGTCA
XM_017023734.1:c.334+169_334+173delinsTGTCA XP_016879223.1:n.334+169_334+173delinsTGTCA
NM_001377486.1:c.334+169_334+173delinsTGTCA NP_001364415.1:n.334+169_334+173delinsTGTCA
NM_022041.4:c.973+169_973+173delinsTGTCA MANE Select NP_071324.1:n.973+169_973+173delinsTGTCA