Canonical Allele Identifier: CA724645538

Gene: GAN

Linked Data

• dbSNP Id: rs1355687284
• gnomAD v3: 16-81315013-A-AGCCGG
• gnomAD v4: 16-81315013-A-AGCCGG
• MyVariant Identifiers: chr16:g.81348618_81348619insGCCGG (hg19) ; chr16:g.81315013_81315014insGCCGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81315021_81315025dup , CM000678.2:g.81315021_81315025dup	GRCh38
NC_000016.9:g.81348626_81348630dup , CM000678.1:g.81348626_81348630dup	GRCh37
NC_000016.8:g.79906127_79906131dup	NCBI36
NG_009007.1:g.5056_5060dup , LRG_242:g.5056_5060dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.-93_-89dup	ENSP00000498114.1:n.-93_-89dup
ENST00000648994.2:c.-93_-89dup MANE Select	ENSP00000497351.1:n.-93_-89dup
ENST00000674788.1:n.33_37dup
ENST00000568107.2:c.-93_-89dup	ENSP00000476795.1:n.-93_-89dup
NM_022041.3:c.-93_-89dup , LRG_242t1:c.-93_-89dup	NP_071324.1:n.-93_-89dup
XM_017023734.1:c.-617_-613dup	XP_016879223.1:n.-617_-613dup
NM_001377486.1:c.-617_-613dup	NP_001364415.1:n.-617_-613dup
NM_022041.4:c.-93_-89dup MANE Select	NP_071324.1:n.-93_-89dup