Canonical Allele Identifier: CA2518088187
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354248_81354249insG , CM000678.2:g.81354248_81354249insG GRCh38
NC_000016.9:g.81387853_81387854insG , CM000678.1:g.81387853_81387854insG GRCh37
NC_000016.8:g.79945354_79945355insG NCBI36
NG_009007.1:g.44283_44284insG , LRG_242:g.44283_44284insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.168-157_168-156insG ENSP00000498114.1:n.168-157_168-156insG
ENST00000648994.2:c.283-157_283-156insG MANE Select ENSP00000497351.1:n.283-157_283-156insG
ENST00000650388.1:c.168-2537_168-2536insG ENSP00000498081.1:n.168-2537_168-2536insG
ENST00000674788.1:n.408-157_408-156insG
ENST00000568107.2:c.283-157_283-156insG ENSP00000476795.1:n.283-157_283-156insG
NM_022041.3:c.283-157_283-156insG , LRG_242t1:c.283-157_283-156insG NP_071324.1:n.283-157_283-156insG
XM_017023734.1:c.-357-157_-357-156insG XP_016879223.1:n.-357-157_-357-156insG
NM_001377486.1:c.-357-157_-357-156insG NP_001364415.1:n.-357-157_-357-156insG
NM_022041.4:c.283-157_283-156insG MANE Select NP_071324.1:n.283-157_283-156insG