Canonical Allele Identifier: CA2634487594
Gene: GAN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315388_81315393del , CM000678.2:g.81315388_81315393del GRCh38
NC_000016.9:g.81348993_81348998del , CM000678.1:g.81348993_81348998del GRCh37
NC_000016.8:g.79906494_79906499del NCBI36
NG_009007.1:g.5423_5428del , LRG_242:g.5423_5428del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.167+108_167+113del ENSP00000498114.1:n.167+108_167+113del
ENST00000648994.2:c.167+108_167+113del MANE Select ENSP00000497351.1:n.167+108_167+113del
ENST00000650388.1:c.167+108_167+113del ENSP00000498081.1:n.167+108_167+113del
ENST00000674788.1:n.292+108_292+113del
ENST00000568107.2:c.167+108_167+113del ENSP00000476795.1:n.167+108_167+113del
NM_022041.3:c.167+108_167+113del , LRG_242t1:c.167+108_167+113del NP_071324.1:n.167+108_167+113del
XM_017023734.1:c.-358+108_-358+113del XP_016879223.1:n.-358+108_-358+113del
NM_001377486.1:c.-358+108_-358+113del NP_001364415.1:n.-358+108_-358+113del
NM_022041.4:c.167+108_167+113del MANE Select NP_071324.1:n.167+108_167+113del