Canonical Allele Identifier: CA2673183087

Gene: ADCY2

Linked Data

• gnomAD v4: 5-7520638-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7520638_7520639insG , CM000667.2:g.7520638_7520639insG	GRCh38
NC_000005.9:g.7520751_7520752insG , CM000667.1:g.7520751_7520752insG	GRCh37
NC_000005.8:g.7573751_7573752insG	NCBI36
NG_046913.1:g.129409_129410insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338316.9:c.409-100_409-99insG MANE Select	ENSP00000342952.4:n.409-100_409-99insG
ENST00000338316.8:c.409-100_409-99insG	ENSP00000342952.4:n.409-100_409-99insG
ENST00000484965.5:n.143-100_143-99insG
ENST00000498598.1:n.108-100_108-99insG
ENST00000537121.5:c.409-100_409-99insG	ENSP00000444803.2:n.409-100_409-99insG
NM_020546.2:c.409-100_409-99insG	NP_065433.2:n.409-100_409-99insG
XM_011513942.1:c.409-100_409-99insG	XP_011512244.1:n.409-100_409-99insG
XR_427657.2:n.423-100_423-99insG
XM_011513942.2:c.409-100_409-99insG	XP_011512244.1:n.409-100_409-99insG
XR_001741973.1:n.423-100_423-99insG
XR_001741974.2:n.423-100_423-99insG
NM_020546.3:c.409-100_409-99insG MANE Select	NP_065433.2:n.409-100_409-99insG