Canonical Allele Identifier: CA1819965902

Gene: ADCY8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.130795974A= , CM000670.2:g.130795974A=	GRCh38
NC_000008.10:g.131808220A= , CM000670.1:g.131808220A=	GRCh37
NC_000008.9:g.131877402A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000286355.10:c.3060+4452T= MANE Select	ENSP00000286355.5:n.3060+4452T=
ENST00000286355.9:c.3060+4452T=	ENSP00000286355.5:n.3060+4452T=
ENST00000377928.7:c.2667+4452T=	ENSP00000367161.3:n.2667+4452T=
NM_001115.2:c.3060+4452T=	NP_001106.1:n.3060+4452T=
XM_005250769.2:c.2970+4452T=	XP_005250826.1:n.2970+4452T=
XM_006716501.2:c.2862+4452T=	XP_006716564.1:n.2862+4452T=
XM_005250769.3:c.2970+4452T=	XP_005250826.1:n.2970+4452T=
XM_006716501.3:c.2862+4452T=	XP_006716564.1:n.2862+4452T=
XM_017013006.1:c.2772+4452T=	XP_016868495.1:n.2772+4452T=
NM_001115.3:c.3060+4452T= MANE Select	NP_001106.1:n.3060+4452T=