Canonical Allele Identifier: CA2237043148
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81358120G= , CM000678.2:g.81358120G= GRCh38
NC_000016.9:g.81391725G= , CM000678.1:g.81391725G= GRCh37
NC_000016.8:g.79949226G= NCBI36
NG_009007.1:g.48155G= , LRG_242:g.48155G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.*681+189G= ENSP00000498114.1:n.*681+189G=
ENST00000648994.2:c.973+189G= MANE Select ENSP00000497351.1:n.973+189G=
ENST00000650388.1:c.507+189G= ENSP00000498081.1:n.507+189G=
ENST00000568107.2:c.973+189G= ENSP00000476795.1:n.973+189G=
NM_022041.3:c.973+189G= , LRG_242t1:c.973+189G= NP_071324.1:n.973+189G=
XM_017023734.1:c.334+189G= XP_016879223.1:n.334+189G=
NM_001377486.1:c.334+189G= NP_001364415.1:n.334+189G=
NM_022041.4:c.973+189G= MANE Select NP_071324.1:n.973+189G=