Canonical Allele Identifier: CA1525712220

Gene: ADCY2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7650188_7650190delinsCTT , CM000667.2:g.7650188_7650190delinsCTT	GRCh38
NC_000005.9:g.7650301_7650303delinsCTT , CM000667.1:g.7650301_7650303delinsCTT	GRCh37
NC_000005.8:g.7703301_7703303delinsCTT	NCBI36
NG_046913.1:g.258959_258961delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338316.9:c.720+23872_720+23874delinsCTT MANE Select	ENSP00000342952.4:n.720+23872_720+23874delinsCTT
ENST00000338316.8:c.720+23872_720+23874delinsCTT	ENSP00000342952.4:n.720+23872_720+23874delinsCTT
ENST00000498598.1:n.420-7838_420-7836delinsCTT
ENST00000515681.1:c.87+23872_87+23874delinsCTT	ENSP00000425069.1:n.87+23872_87+23874delinsCTT
ENST00000537121.5:c.714+23872_714+23874delinsCTT	ENSP00000444803.2:n.714+23872_714+23874delinsCTT
NM_020546.2:c.720+23872_720+23874delinsCTT	NP_065433.2:n.720+23872_720+23874delinsCTT
XM_011513942.1:c.720+23872_720+23874delinsCTT	XP_011512244.1:n.720+23872_720+23874delinsCTT
XR_427657.2:n.734+23872_734+23874delinsCTT
XM_011513942.2:c.720+23872_720+23874delinsCTT	XP_011512244.1:n.720+23872_720+23874delinsCTT
XR_001741973.1:n.734+23872_734+23874delinsCTT
XR_001741974.2:n.734+23872_734+23874delinsCTT
NM_020546.3:c.720+23872_720+23874delinsCTT MANE Select	NP_065433.2:n.720+23872_720+23874delinsCTT