Canonical Allele Identifier: CA1819965824

Gene: ADCY8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.130795784_130795785delinsTG , CM000670.2:g.130795784_130795785delinsTG	GRCh38
NC_000008.10:g.131808030_131808031delinsTG , CM000670.1:g.131808030_131808031delinsTG	GRCh37
NC_000008.9:g.131877212_131877213delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286355.10:c.3060+4641_3060+4642delinsCA MANE Select	ENSP00000286355.5:n.3060+4641_3060+4642delinsCA
ENST00000286355.9:c.3060+4641_3060+4642delinsCA	ENSP00000286355.5:n.3060+4641_3060+4642delinsCA
ENST00000377928.7:c.2667+4641_2667+4642delinsCA	ENSP00000367161.3:n.2667+4641_2667+4642delinsCA
NM_001115.2:c.3060+4641_3060+4642delinsCA	NP_001106.1:n.3060+4641_3060+4642delinsCA
XM_005250769.2:c.2970+4641_2970+4642delinsCA	XP_005250826.1:n.2970+4641_2970+4642delinsCA
XM_006716501.2:c.2862+4641_2862+4642delinsCA	XP_006716564.1:n.2862+4641_2862+4642delinsCA
XM_005250769.3:c.2970+4641_2970+4642delinsCA	XP_005250826.1:n.2970+4641_2970+4642delinsCA
XM_006716501.3:c.2862+4641_2862+4642delinsCA	XP_006716564.1:n.2862+4641_2862+4642delinsCA
XM_017013006.1:c.2772+4641_2772+4642delinsCA	XP_016868495.1:n.2772+4641_2772+4642delinsCA
NM_001115.3:c.3060+4641_3060+4642delinsCA MANE Select	NP_001106.1:n.3060+4641_3060+4642delinsCA