Canonical Allele Identifier: CA2634487601

Gene: GAN

Linked Data

• gnomAD v4: 16-81315389-GGGTCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81315390_81315394del , CM000678.2:g.81315390_81315394del	GRCh38
NC_000016.9:g.81348995_81348999del , CM000678.1:g.81348995_81348999del	GRCh37
NC_000016.8:g.79906496_79906500del	NCBI36
NG_009007.1:g.5425_5429del , LRG_242:g.5425_5429del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.167+110_167+114del	ENSP00000498114.1:n.167+110_167+114del
ENST00000648994.2:c.167+110_167+114del MANE Select	ENSP00000497351.1:n.167+110_167+114del
ENST00000650388.1:c.167+110_167+114del	ENSP00000498081.1:n.167+110_167+114del
ENST00000674788.1:n.292+110_292+114del
ENST00000568107.2:c.167+110_167+114del	ENSP00000476795.1:n.167+110_167+114del
NM_022041.3:c.167+110_167+114del , LRG_242t1:c.167+110_167+114del	NP_071324.1:n.167+110_167+114del
XM_017023734.1:c.-358+110_-358+114del	XP_016879223.1:n.-358+110_-358+114del
NM_001377486.1:c.-358+110_-358+114del	NP_001364415.1:n.-358+110_-358+114del
NM_022041.4:c.167+110_167+114del MANE Select	NP_071324.1:n.167+110_167+114del