Canonical Allele Identifier: CA813941579

Gene: ADCY2

Linked Data

• dbSNP Id: rs1341706282
• MyVariant Identifiers: chr5:g.7530738_7530739insG (hg19) ; chr5:g.7530625_7530626insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7530625_7530626insG , CM000667.2:g.7530625_7530626insG	GRCh38
NC_000005.9:g.7530738_7530739insG , CM000667.1:g.7530738_7530739insG	GRCh37
NC_000005.8:g.7583738_7583739insG	NCBI36
NG_046913.1:g.139396_139397insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338316.9:c.570+9726_570+9727insG MANE Select	ENSP00000342952.4:n.570+9726_570+9727insG
ENST00000338316.8:c.570+9726_570+9727insG	ENSP00000342952.4:n.570+9726_570+9727insG
ENST00000498598.1:n.269+9726_269+9727insG
ENST00000537121.5:c.565+9726_565+9727insG	ENSP00000444803.2:n.565+9726_565+9727insG
NM_020546.2:c.570+9726_570+9727insG	NP_065433.2:n.570+9726_570+9727insG
XM_011513942.1:c.570+9726_570+9727insG	XP_011512244.1:n.570+9726_570+9727insG
XR_427657.2:n.584+9726_584+9727insG
XM_011513942.2:c.570+9726_570+9727insG	XP_011512244.1:n.570+9726_570+9727insG
XR_001741973.1:n.584+9726_584+9727insG
XR_001741974.2:n.584+9726_584+9727insG
NM_020546.3:c.570+9726_570+9727insG MANE Select	NP_065433.2:n.570+9726_570+9727insG