Canonical Allele Identifier: CA4878448

Gene: ADCY8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.131039553C>T , CM000670.2:g.131039553C>T	GRCh38
NC_000008.10:g.132051799C>T , CM000670.1:g.132051799C>T	GRCh37
NC_000008.9:g.132120981C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286355.10:c.781G>A MANE Select	ENSP00000286355.5:p.Gly261Ser
ENST00000286355.9:c.781G>A	ENSP00000286355.5:p.Gly261Ser
ENST00000377928.7:c.781G>A	ENSP00000367161.3:p.Gly261Ser
NM_001115.2:c.781G>A	NP_001106.1:p.Gly261Ser
XM_005250769.2:c.781G>A	XP_005250826.1:p.Gly261Ser
XM_006716501.2:c.781G>A	XP_006716564.1:p.Gly261Ser
XR_928651.1:n.20C>T
XR_928652.1:n.32C>T
XR_928653.1:n.20C>T
XM_005250769.3:c.781G>A	XP_005250826.1:p.Gly261Ser
XM_006716501.3:c.781G>A	XP_006716564.1:p.Gly261Ser
XM_017013006.1:c.781G>A	XP_016868495.1:p.Gly261Ser
XM_017013007.1:c.781G>A	XP_016868496.1:p.Gly261Ser
XR_001746087.1:n.32C>T
XR_928651.2:n.24C>T
XR_928653.2:n.24C>T
NM_001115.3:c.781G>A MANE Select	NP_001106.1:p.Gly261Ser