Canonical Allele Identifier: CA623755769

Gene: GAN

Linked Data

• dbSNP Id: rs1397140079
• gnomAD v2: 16-81391780-A-G
• gnomAD v3: 16-81358175-A-G
• gnomAD v4: 16-81358175-A-G
• MyVariant Identifiers: chr16:g.81391780A>G (hg19) ; chr16:g.81358175A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81358175A>G , CM000678.2:g.81358175A>G	GRCh38
NC_000016.9:g.81391780A>G , CM000678.1:g.81391780A>G	GRCh37
NC_000016.8:g.79949281A>G	NCBI36
NG_009007.1:g.48210A>G , LRG_242:g.48210A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.*681+244A>G	ENSP00000498114.1:n.*681+244A>G
ENST00000648994.2:c.973+244A>G MANE Select	ENSP00000497351.1:n.973+244A>G
ENST00000650388.1:c.507+244A>G	ENSP00000498081.1:n.507+244A>G
ENST00000568107.2:c.973+244A>G	ENSP00000476795.1:n.973+244A>G
NM_022041.3:c.973+244A>G , LRG_242t1:c.973+244A>G	NP_071324.1:n.973+244A>G
XM_017023734.1:c.334+244A>G	XP_016879223.1:n.334+244A>G
NM_001377486.1:c.334+244A>G	NP_001364415.1:n.334+244A>G
NM_022041.4:c.973+244A>G MANE Select	NP_071324.1:n.973+244A>G