Canonical Allele Identifier: CA2634487565

Gene: GAN

Linked Data

• gnomAD v4: 16-81315359-C-CGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81315359_81315360insGG , CM000678.2:g.81315359_81315360insGG	GRCh38
NC_000016.9:g.81348964_81348965insGG , CM000678.1:g.81348964_81348965insGG	GRCh37
NC_000016.8:g.79906465_79906466insGG	NCBI36
NG_009007.1:g.5394_5395insGG , LRG_242:g.5394_5395insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.167+79_167+80insGG	ENSP00000498114.1:n.167+79_167+80insGG
ENST00000648994.2:c.167+79_167+80insGG MANE Select	ENSP00000497351.1:n.167+79_167+80insGG
ENST00000650388.1:c.167+79_167+80insGG	ENSP00000498081.1:n.167+79_167+80insGG
ENST00000674788.1:n.292+79_292+80insGG
ENST00000568107.2:c.167+79_167+80insGG	ENSP00000476795.1:n.167+79_167+80insGG
NM_022041.3:c.167+79_167+80insGG , LRG_242t1:c.167+79_167+80insGG	NP_071324.1:n.167+79_167+80insGG
XM_017023734.1:c.-358+79_-358+80insGG	XP_016879223.1:n.-358+79_-358+80insGG
NM_001377486.1:c.-358+79_-358+80insGG	NP_001364415.1:n.-358+79_-358+80insGG
NM_022041.4:c.167+79_167+80insGG MANE Select	NP_071324.1:n.167+79_167+80insGG