Canonical Allele Identifier: CA1525635519

Gene: ADCY2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7517176_7517177delinsCT , CM000667.2:g.7517176_7517177delinsCT	GRCh38
NC_000005.9:g.7517289_7517290delinsCT , CM000667.1:g.7517289_7517290delinsCT	GRCh37
NC_000005.8:g.7570289_7570290delinsCT	NCBI36
NG_046913.1:g.125947_125948delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338316.9:c.409-3562_409-3561delinsCT MANE Select	ENSP00000342952.4:n.409-3562_409-3561delinsCT
ENST00000338316.8:c.409-3562_409-3561delinsCT	ENSP00000342952.4:n.409-3562_409-3561delinsCT
ENST00000484965.5:n.143-3562_143-3561delinsCT
ENST00000498598.1:n.108-3562_108-3561delinsCT
ENST00000537121.5:c.409-3562_409-3561delinsCT	ENSP00000444803.2:n.409-3562_409-3561delinsCT
NM_020546.2:c.409-3562_409-3561delinsCT	NP_065433.2:n.409-3562_409-3561delinsCT
XM_011513942.1:c.409-3562_409-3561delinsCT	XP_011512244.1:n.409-3562_409-3561delinsCT
XR_427657.2:n.423-3562_423-3561delinsCT
XM_011513942.2:c.409-3562_409-3561delinsCT	XP_011512244.1:n.409-3562_409-3561delinsCT
XR_001741973.1:n.423-3562_423-3561delinsCT
XR_001741974.2:n.423-3562_423-3561delinsCT
NM_020546.3:c.409-3562_409-3561delinsCT MANE Select	NP_065433.2:n.409-3562_409-3561delinsCT