Canonical Allele Identifier: CA2634487894

Gene: GAN

Linked Data

• gnomAD v4: 16-81354396-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81354402dup , CM000678.2:g.81354402dup	GRCh38
NC_000016.9:g.81388007dup , CM000678.1:g.81388007dup	GRCh37
NC_000016.8:g.79945508dup	NCBI36
NG_009007.1:g.44437dup , LRG_242:g.44437dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.168-3dup	ENSP00000498114.1:n.168-3dup
ENST00000648994.2:c.283-3dup MANE Select	ENSP00000497351.1:n.283-3dup
ENST00000650388.1:c.168-2383dup	ENSP00000498081.1:n.168-2383dup
ENST00000674788.1:n.408-3dup
ENST00000568107.2:c.283-3dup	ENSP00000476795.1:n.283-3dup
NM_022041.3:c.283-3dup , LRG_242t1:c.283-3dup	NP_071324.1:n.283-3dup
XM_017023734.1:c.-357-3dup	XP_016879223.1:n.-357-3dup
NM_001377486.1:c.-357-3dup	NP_001364415.1:n.-357-3dup
NM_022041.4:c.283-3dup MANE Select	NP_071324.1:n.283-3dup