Canonical Allele Identifier: CA2634489291

Gene: GAN

Linked Data

• gnomAD v4: 16-81365318-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81365318T>A , CM000678.2:g.81365318T>A	GRCh38
NC_000016.9:g.81398923T>A , CM000678.1:g.81398923T>A	GRCh37
NC_000016.8:g.79956424T>A	NCBI36
NG_009007.1:g.55353T>A , LRG_242:g.55353T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.*1082-32T>A	ENSP00000498114.1:n.*1082-32T>A
ENST00000648994.2:c.1374-32T>A MANE Select	ENSP00000497351.1:n.1374-32T>A
ENST00000650388.1:c.908-32T>A	ENSP00000498081.1:n.908-32T>A
ENST00000568107.2:c.1374-32T>A	ENSP00000476795.1:n.1374-32T>A
NM_022041.3:c.1374-32T>A , LRG_242t1:c.1374-32T>A	NP_071324.1:n.1374-32T>A
XM_017023734.1:c.735-32T>A	XP_016879223.1:n.735-32T>A
NM_001377486.1:c.735-32T>A	NP_001364415.1:n.735-32T>A
NM_022041.4:c.1374-32T>A MANE Select	NP_071324.1:n.1374-32T>A