Canonical Allele Identifier: CA1819965942

Gene: ADCY8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.130796075_130796076delinsCT , CM000670.2:g.130796075_130796076delinsCT	GRCh38
NC_000008.10:g.131808321_131808322delinsCT , CM000670.1:g.131808321_131808322delinsCT	GRCh37
NC_000008.9:g.131877503_131877504delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286355.10:c.3060+4350_3060+4351delinsAG MANE Select	ENSP00000286355.5:n.3060+4350_3060+4351delinsAG
ENST00000286355.9:c.3060+4350_3060+4351delinsAG	ENSP00000286355.5:n.3060+4350_3060+4351delinsAG
ENST00000377928.7:c.2667+4350_2667+4351delinsAG	ENSP00000367161.3:n.2667+4350_2667+4351delinsAG
NM_001115.2:c.3060+4350_3060+4351delinsAG	NP_001106.1:n.3060+4350_3060+4351delinsAG
XM_005250769.2:c.2970+4350_2970+4351delinsAG	XP_005250826.1:n.2970+4350_2970+4351delinsAG
XM_006716501.2:c.2862+4350_2862+4351delinsAG	XP_006716564.1:n.2862+4350_2862+4351delinsAG
XM_005250769.3:c.2970+4350_2970+4351delinsAG	XP_005250826.1:n.2970+4350_2970+4351delinsAG
XM_006716501.3:c.2862+4350_2862+4351delinsAG	XP_006716564.1:n.2862+4350_2862+4351delinsAG
XM_017013006.1:c.2772+4350_2772+4351delinsAG	XP_016868495.1:n.2772+4350_2772+4351delinsAG
NM_001115.3:c.3060+4350_3060+4351delinsAG MANE Select	NP_001106.1:n.3060+4350_3060+4351delinsAG