Canonical Allele Identifier: CA767118259

Gene: ADCY3

Linked Data

• dbSNP Id: rs1417471686
• MyVariant Identifiers: chr2:g.25047492_25047494del (hg19) ; chr2:g.24824623_24824625del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824624_24824626del , CM000664.2:g.24824624_24824626del	GRCh38
NC_000002.11:g.25047493_25047495del , CM000664.1:g.25047493_25047495del	GRCh37
NC_000002.10:g.24900997_24900999del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2581-89_2581-87del	ENSP00000384484.2:n.2581-89_2581-87del
ENST00000679454.1:c.2578-89_2578-87del MANE Select	ENSP00000505261.1:n.2578-89_2578-87del
ENST00000260600.9:c.2578-89_2578-87del	ENSP00000260600.5:n.2578-89_2578-87del
ENST00000405392.5:c.2581-89_2581-87del	ENSP00000384484.2:n.2581-89_2581-87del
ENST00000606682.5:c.1519-89_1519-87del	ENSP00000475652.1:n.1519-89_1519-87del
NM_004036.3:c.2578-89_2578-87del	NP_004027.2:n.2578-89_2578-87del
XM_005264104.1:c.2581-89_2581-87del	XP_005264161.1:n.2581-89_2581-87del
XM_005264105.1:c.2578-89_2578-87del	XP_005264162.1:n.2578-89_2578-87del
XM_006711925.1:c.2647-89_2647-87del	XP_006711988.1:n.2647-89_2647-87del
XM_011532489.1:c.2704-89_2704-87del	XP_011530791.1:n.2704-89_2704-87del
XM_011532490.1:c.2701-89_2701-87del	XP_011530792.1:n.2701-89_2701-87del
XM_011532491.1:c.2638-89_2638-87del	XP_011530793.1:n.2638-89_2638-87del
XM_011532492.1:c.2704-89_2704-87del	XP_011530794.1:n.2704-89_2704-87del
XM_011532493.1:c.2566-89_2566-87del	XP_011530795.1:n.2566-89_2566-87del
XM_011532494.1:c.2506-89_2506-87del	XP_011530796.1:n.2506-89_2506-87del
XM_011532495.1:c.2038-89_2038-87del	XP_011530797.1:n.2038-89_2038-87del
XM_011532496.1:c.1981-89_1981-87del	XP_011530798.1:n.1981-89_1981-87del
NM_001320613.1:c.2581-89_2581-87del	NP_001307542.1:n.2581-89_2581-87del
NM_004036.4:c.2578-89_2578-87del	NP_004027.2:n.2578-89_2578-87del
XM_011532492.2:c.2704-89_2704-87del	XP_011530794.1:n.2704-89_2704-87del
XM_017003186.1:c.2644-89_2644-87del	XP_016858675.1:n.2644-89_2644-87del
XM_017003187.1:c.2635-89_2635-87del	XP_016858676.1:n.2635-89_2635-87del
XM_017003188.1:c.2701-89_2701-87del	XP_016858677.1:n.2701-89_2701-87del
XM_017003189.1:c.2563-89_2563-87del	XP_016858678.1:n.2563-89_2563-87del
XM_017003190.1:c.2440-89_2440-87del	XP_016858679.1:n.2440-89_2440-87del
XM_017003191.1:c.2068-89_2068-87del	XP_016858680.1:n.2068-89_2068-87del
XM_017003192.1:c.1858-89_1858-87del	XP_016858681.1:n.1858-89_1858-87del
XM_017003193.1:c.1855-89_1855-87del	XP_016858682.1:n.1855-89_1855-87del
NM_001320613.2:c.2581-89_2581-87del	NP_001307542.1:n.2581-89_2581-87del
NM_001377128.1:c.2644-89_2644-87del	NP_001364057.1:n.2644-89_2644-87del
NM_001377129.1:c.2440-89_2440-87del	NP_001364058.1:n.2440-89_2440-87del
NM_001377130.1:c.2173-89_2173-87del	NP_001364059.1:n.2173-89_2173-87del
NM_001377131.1:c.1855-89_1855-87del	NP_001364060.1:n.1855-89_1855-87del
NM_001377132.1:c.2578-89_2578-87del	NP_001364061.1:n.2578-89_2578-87del
NM_004036.5:c.2578-89_2578-87del MANE Select	NP_004027.2:n.2578-89_2578-87del