Canonical Allele Identifier: CA1525635613

Gene: ADCY2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7517268_7517270delinsCTT , CM000667.2:g.7517268_7517270delinsCTT	GRCh38
NC_000005.9:g.7517381_7517383delinsCTT , CM000667.1:g.7517381_7517383delinsCTT	GRCh37
NC_000005.8:g.7570381_7570383delinsCTT	NCBI36
NG_046913.1:g.126039_126041delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338316.9:c.409-3470_409-3468delinsCTT MANE Select	ENSP00000342952.4:n.409-3470_409-3468delinsCTT
ENST00000338316.8:c.409-3470_409-3468delinsCTT	ENSP00000342952.4:n.409-3470_409-3468delinsCTT
ENST00000484965.5:n.143-3470_143-3468delinsCTT
ENST00000498598.1:n.108-3470_108-3468delinsCTT
ENST00000537121.5:c.409-3470_409-3468delinsCTT	ENSP00000444803.2:n.409-3470_409-3468delinsCTT
NM_020546.2:c.409-3470_409-3468delinsCTT	NP_065433.2:n.409-3470_409-3468delinsCTT
XM_011513942.1:c.409-3470_409-3468delinsCTT	XP_011512244.1:n.409-3470_409-3468delinsCTT
XR_427657.2:n.423-3470_423-3468delinsCTT
XM_011513942.2:c.409-3470_409-3468delinsCTT	XP_011512244.1:n.409-3470_409-3468delinsCTT
XR_001741973.1:n.423-3470_423-3468delinsCTT
XR_001741974.2:n.423-3470_423-3468delinsCTT
NM_020546.3:c.409-3470_409-3468delinsCTT MANE Select	NP_065433.2:n.409-3470_409-3468delinsCTT