Canonical Allele Identifier: CA2807834292
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81358107_81358108insAA , CM000678.2:g.81358107_81358108insAA GRCh38
NC_000016.9:g.81391712_81391713insAA , CM000678.1:g.81391712_81391713insAA GRCh37
NC_000016.8:g.79949213_79949214insAA NCBI36
NG_009007.1:g.48142_48143insAA , LRG_242:g.48142_48143insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.*681+176_*681+177insAA ENSP00000498114.1:n.*681+176_*681+177insAA
ENST00000648994.2:c.973+176_973+177insAA MANE Select ENSP00000497351.1:n.973+176_973+177insAA
ENST00000650388.1:c.507+176_507+177insAA ENSP00000498081.1:n.507+176_507+177insAA
ENST00000568107.2:c.973+176_973+177insAA ENSP00000476795.1:n.973+176_973+177insAA
NM_022041.3:c.973+176_973+177insAA , LRG_242t1:c.973+176_973+177insAA NP_071324.1:n.973+176_973+177insAA
XM_017023734.1:c.334+176_334+177insAA XP_016879223.1:n.334+176_334+177insAA
NM_001377486.1:c.334+176_334+177insAA NP_001364415.1:n.334+176_334+177insAA
NM_022041.4:c.973+176_973+177insAA MANE Select NP_071324.1:n.973+176_973+177insAA