Canonical Allele Identifier: CA814014636

Gene: ADCY2

Linked Data

• dbSNP Id: rs1409882182
• MyVariant Identifiers: chr5:g.7650302_7650303del (hg19) ; chr5:g.7650189_7650190del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7650190_7650191del , CM000667.2:g.7650190_7650191del	GRCh38
NC_000005.9:g.7650303_7650304del , CM000667.1:g.7650303_7650304del	GRCh37
NC_000005.8:g.7703303_7703304del	NCBI36
NG_046913.1:g.258961_258962del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338316.9:c.720+23874_720+23875del MANE Select	ENSP00000342952.4:n.720+23874_720+23875del
ENST00000338316.8:c.720+23874_720+23875del	ENSP00000342952.4:n.720+23874_720+23875del
ENST00000498598.1:n.420-7836_420-7835del
ENST00000515681.1:c.87+23874_87+23875del	ENSP00000425069.1:n.87+23874_87+23875del
ENST00000537121.5:c.714+23874_714+23875del	ENSP00000444803.2:n.714+23874_714+23875del
NM_020546.2:c.720+23874_720+23875del	NP_065433.2:n.720+23874_720+23875del
XM_011513942.1:c.720+23874_720+23875del	XP_011512244.1:n.720+23874_720+23875del
XR_427657.2:n.734+23874_734+23875del
XM_011513942.2:c.720+23874_720+23875del	XP_011512244.1:n.720+23874_720+23875del
XR_001741973.1:n.734+23874_734+23875del
XR_001741974.2:n.734+23874_734+23875del
NM_020546.3:c.720+23874_720+23875del MANE Select	NP_065433.2:n.720+23874_720+23875del