Canonical Allele Identifier: CA2634487604

Gene: GAN

Linked Data

• gnomAD v4: 16-81315390-GGTCCCCGCGTCACCGTTGGCGCGGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81315396_81315420del , CM000678.2:g.81315396_81315420del	GRCh38
NC_000016.9:g.81349001_81349025del , CM000678.1:g.81349001_81349025del	GRCh37
NC_000016.8:g.79906502_79906526del	NCBI36
NG_009007.1:g.5431_5455del , LRG_242:g.5431_5455del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.167+116_167+140del	ENSP00000498114.1:n.167+116_167+140del
ENST00000648994.2:c.167+116_167+140del MANE Select	ENSP00000497351.1:n.167+116_167+140del
ENST00000650388.1:c.167+116_167+140del	ENSP00000498081.1:n.167+116_167+140del
ENST00000674788.1:n.292+116_292+140del
ENST00000568107.2:c.167+116_167+140del	ENSP00000476795.1:n.167+116_167+140del
NM_022041.3:c.167+116_167+140del , LRG_242t1:c.167+116_167+140del	NP_071324.1:n.167+116_167+140del
XM_017023734.1:c.-358+116_-358+140del	XP_016879223.1:n.-358+116_-358+140del
NM_001377486.1:c.-358+116_-358+140del	NP_001364415.1:n.-358+116_-358+140del
NM_022041.4:c.167+116_167+140del MANE Select	NP_071324.1:n.167+116_167+140del