Canonical Allele Identifier: CA623755157

Gene: GAN

Linked Data

• dbSNP Id: rs1177600498
• gnomAD v2: 16-81387887-C-G
• gnomAD v3: 16-81354282-C-G
• gnomAD v4: 16-81354282-C-G
• MyVariant Identifiers: chr16:g.81387887C>G (hg19) ; chr16:g.81354282C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81354282C>G , CM000678.2:g.81354282C>G	GRCh38
NC_000016.9:g.81387887C>G , CM000678.1:g.81387887C>G	GRCh37
NC_000016.8:g.79945388C>G	NCBI36
NG_009007.1:g.44317C>G , LRG_242:g.44317C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.168-123C>G	ENSP00000498114.1:n.168-123C>G
ENST00000648994.2:c.283-123C>G MANE Select	ENSP00000497351.1:n.283-123C>G
ENST00000650388.1:c.168-2503C>G	ENSP00000498081.1:n.168-2503C>G
ENST00000674788.1:n.408-123C>G
ENST00000568107.2:c.283-123C>G	ENSP00000476795.1:n.283-123C>G
NM_022041.3:c.283-123C>G , LRG_242t1:c.283-123C>G	NP_071324.1:n.283-123C>G
XM_017023734.1:c.-357-123C>G	XP_016879223.1:n.-357-123C>G
NM_001377486.1:c.-357-123C>G	NP_001364415.1:n.-357-123C>G
NM_022041.4:c.283-123C>G MANE Select	NP_071324.1:n.283-123C>G