Canonical Allele Identifier: CA43683519

Gene: ADCY3

Linked Data

• dbSNP Id: rs969573784
• gnomAD v3: 2-24824744-CCGGGCATGGTGG-C
• gnomAD v4: 2-24824744-CCGGGCATGGTGG-C
• MyVariant Identifiers: chr2:g.25047614_25047625del (hg19) ; chr2:g.24824745_24824756del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824751_24824762del , CM000664.2:g.24824751_24824762del	GRCh38
NC_000002.11:g.25047620_25047631del , CM000664.1:g.25047620_25047631del	GRCh37
NC_000002.10:g.24901124_24901135del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2581-220_2581-209del	ENSP00000384484.2:n.2581-220_2581-209del
ENST00000679454.1:c.2578-220_2578-209del MANE Select	ENSP00000505261.1:n.2578-220_2578-209del
ENST00000260600.9:c.2578-220_2578-209del	ENSP00000260600.5:n.2578-220_2578-209del
ENST00000405392.5:c.2581-220_2581-209del	ENSP00000384484.2:n.2581-220_2581-209del
ENST00000606682.5:c.1519-220_1519-209del	ENSP00000475652.1:n.1519-220_1519-209del
NM_004036.3:c.2578-220_2578-209del	NP_004027.2:n.2578-220_2578-209del
XM_005264104.1:c.2581-220_2581-209del	XP_005264161.1:n.2581-220_2581-209del
XM_005264105.1:c.2578-220_2578-209del	XP_005264162.1:n.2578-220_2578-209del
XM_006711925.1:c.2647-220_2647-209del	XP_006711988.1:n.2647-220_2647-209del
XM_011532489.1:c.2704-220_2704-209del	XP_011530791.1:n.2704-220_2704-209del
XM_011532490.1:c.2701-220_2701-209del	XP_011530792.1:n.2701-220_2701-209del
XM_011532491.1:c.2638-220_2638-209del	XP_011530793.1:n.2638-220_2638-209del
XM_011532492.1:c.2704-220_2704-209del	XP_011530794.1:n.2704-220_2704-209del
XM_011532493.1:c.2566-220_2566-209del	XP_011530795.1:n.2566-220_2566-209del
XM_011532494.1:c.2506-220_2506-209del	XP_011530796.1:n.2506-220_2506-209del
XM_011532495.1:c.2038-220_2038-209del	XP_011530797.1:n.2038-220_2038-209del
XM_011532496.1:c.1981-220_1981-209del	XP_011530798.1:n.1981-220_1981-209del
NM_001320613.1:c.2581-220_2581-209del	NP_001307542.1:n.2581-220_2581-209del
NM_004036.4:c.2578-220_2578-209del	NP_004027.2:n.2578-220_2578-209del
XM_011532492.2:c.2704-220_2704-209del	XP_011530794.1:n.2704-220_2704-209del
XM_017003186.1:c.2644-220_2644-209del	XP_016858675.1:n.2644-220_2644-209del
XM_017003187.1:c.2635-220_2635-209del	XP_016858676.1:n.2635-220_2635-209del
XM_017003188.1:c.2701-220_2701-209del	XP_016858677.1:n.2701-220_2701-209del
XM_017003189.1:c.2563-220_2563-209del	XP_016858678.1:n.2563-220_2563-209del
XM_017003190.1:c.2440-220_2440-209del	XP_016858679.1:n.2440-220_2440-209del
XM_017003191.1:c.2068-220_2068-209del	XP_016858680.1:n.2068-220_2068-209del
XM_017003192.1:c.1858-220_1858-209del	XP_016858681.1:n.1858-220_1858-209del
XM_017003193.1:c.1855-220_1855-209del	XP_016858682.1:n.1855-220_1855-209del
NM_001320613.2:c.2581-220_2581-209del	NP_001307542.1:n.2581-220_2581-209del
NM_001377128.1:c.2644-220_2644-209del	NP_001364057.1:n.2644-220_2644-209del
NM_001377129.1:c.2440-220_2440-209del	NP_001364058.1:n.2440-220_2440-209del
NM_001377130.1:c.2173-220_2173-209del	NP_001364059.1:n.2173-220_2173-209del
NM_001377131.1:c.1855-220_1855-209del	NP_001364060.1:n.1855-220_1855-209del
NM_001377132.1:c.2578-220_2578-209del	NP_001364061.1:n.2578-220_2578-209del
NM_004036.5:c.2578-220_2578-209del MANE Select	NP_004027.2:n.2578-220_2578-209del