Canonical Allele Identifier: CA1819965870

Gene: ADCY8

Linked Data

• dbSNP Id: rs1815565635

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.130795914_130795935del , CM000670.2:g.130795914_130795935del	GRCh38
NC_000008.10:g.131808160_131808181del , CM000670.1:g.131808160_131808181del	GRCh37
NC_000008.9:g.131877342_131877363del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000286355.10:c.3060+4494_3060+4515del MANE Select	ENSP00000286355.5:n.3060+4494_3060+4515de...
ENST00000286355.9:c.3060+4494_3060+4515del	ENSP00000286355.5:n.3060+4494_3060+4515de...
ENST00000377928.7:c.2667+4494_2667+4515del	ENSP00000367161.3:n.2667+4494_2667+4515de...
NM_001115.2:c.3060+4494_3060+4515del	NP_001106.1:n.3060+4494_3060+4515del
XM_005250769.2:c.2970+4494_2970+4515del	XP_005250826.1:n.2970+4494_2970+4515del
XM_006716501.2:c.2862+4494_2862+4515del	XP_006716564.1:n.2862+4494_2862+4515del
XM_005250769.3:c.2970+4494_2970+4515del	XP_005250826.1:n.2970+4494_2970+4515del
XM_006716501.3:c.2862+4494_2862+4515del	XP_006716564.1:n.2862+4494_2862+4515del
XM_017013006.1:c.2772+4494_2772+4515del	XP_016868495.1:n.2772+4494_2772+4515del
NM_001115.3:c.3060+4494_3060+4515del MANE Select	NP_001106.1:n.3060+4494_3060+4515del