Canonical Allele Identifier: CA979655919

Gene: GAN

Linked Data

• dbSNP Id: rs1910411518
• gnomAD v3: 16-81354337-TA-T
• gnomAD v4: 16-81354337-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81354339del , CM000678.2:g.81354339del	GRCh38
NC_000016.9:g.81387944del , CM000678.1:g.81387944del	GRCh37
NC_000016.8:g.79945445del	NCBI36
NG_009007.1:g.44374del , LRG_242:g.44374del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.168-66del	ENSP00000498114.1:n.168-66del
ENST00000648994.2:c.283-66del MANE Select	ENSP00000497351.1:n.283-66del
ENST00000650388.1:c.168-2446del	ENSP00000498081.1:n.168-2446del
ENST00000674788.1:n.408-66del
ENST00000568107.2:c.283-66del	ENSP00000476795.1:n.283-66del
NM_022041.3:c.283-66del , LRG_242t1:c.283-66del	NP_071324.1:n.283-66del
XM_017023734.1:c.-357-66del	XP_016879223.1:n.-357-66del
NM_001377486.1:c.-357-66del	NP_001364415.1:n.-357-66del
NM_022041.4:c.283-66del MANE Select	NP_071324.1:n.283-66del