Canonical Allele Identifier: CA2658140120

Gene: ADCY3

Linked Data

• gnomAD v4: 2-24824564-TGCTCTAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824568_24824574del , CM000664.2:g.24824568_24824574del	GRCh38
NC_000002.11:g.25047437_25047443del , CM000664.1:g.25047437_25047443del	GRCh37
NC_000002.10:g.24900941_24900947del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2581-35_2581-29del	ENSP00000384484.2:n.2581-35_2581-29del
ENST00000679454.1:c.2578-35_2578-29del MANE Select	ENSP00000505261.1:n.2578-35_2578-29del
ENST00000260600.9:c.2578-35_2578-29del	ENSP00000260600.5:n.2578-35_2578-29del
ENST00000405392.5:c.2581-35_2581-29del	ENSP00000384484.2:n.2581-35_2581-29del
ENST00000606682.5:c.1519-35_1519-29del	ENSP00000475652.1:n.1519-35_1519-29del
NM_004036.3:c.2578-35_2578-29del	NP_004027.2:n.2578-35_2578-29del
XM_005264104.1:c.2581-35_2581-29del	XP_005264161.1:n.2581-35_2581-29del
XM_005264105.1:c.2578-35_2578-29del	XP_005264162.1:n.2578-35_2578-29del
XM_006711925.1:c.2647-35_2647-29del	XP_006711988.1:n.2647-35_2647-29del
XM_011532489.1:c.2704-35_2704-29del	XP_011530791.1:n.2704-35_2704-29del
XM_011532490.1:c.2701-35_2701-29del	XP_011530792.1:n.2701-35_2701-29del
XM_011532491.1:c.2638-35_2638-29del	XP_011530793.1:n.2638-35_2638-29del
XM_011532492.1:c.2704-35_2704-29del	XP_011530794.1:n.2704-35_2704-29del
XM_011532493.1:c.2566-35_2566-29del	XP_011530795.1:n.2566-35_2566-29del
XM_011532494.1:c.2506-35_2506-29del	XP_011530796.1:n.2506-35_2506-29del
XM_011532495.1:c.2038-35_2038-29del	XP_011530797.1:n.2038-35_2038-29del
XM_011532496.1:c.1981-35_1981-29del	XP_011530798.1:n.1981-35_1981-29del
NM_001320613.1:c.2581-35_2581-29del	NP_001307542.1:n.2581-35_2581-29del
NM_004036.4:c.2578-35_2578-29del	NP_004027.2:n.2578-35_2578-29del
XM_011532492.2:c.2704-35_2704-29del	XP_011530794.1:n.2704-35_2704-29del
XM_017003186.1:c.2644-35_2644-29del	XP_016858675.1:n.2644-35_2644-29del
XM_017003187.1:c.2635-35_2635-29del	XP_016858676.1:n.2635-35_2635-29del
XM_017003188.1:c.2701-35_2701-29del	XP_016858677.1:n.2701-35_2701-29del
XM_017003189.1:c.2563-35_2563-29del	XP_016858678.1:n.2563-35_2563-29del
XM_017003190.1:c.2440-35_2440-29del	XP_016858679.1:n.2440-35_2440-29del
XM_017003191.1:c.2068-35_2068-29del	XP_016858680.1:n.2068-35_2068-29del
XM_017003192.1:c.1858-35_1858-29del	XP_016858681.1:n.1858-35_1858-29del
XM_017003193.1:c.1855-35_1855-29del	XP_016858682.1:n.1855-35_1855-29del
NM_001320613.2:c.2581-35_2581-29del	NP_001307542.1:n.2581-35_2581-29del
NM_001377128.1:c.2644-35_2644-29del	NP_001364057.1:n.2644-35_2644-29del
NM_001377129.1:c.2440-35_2440-29del	NP_001364058.1:n.2440-35_2440-29del
NM_001377130.1:c.2173-35_2173-29del	NP_001364059.1:n.2173-35_2173-29del
NM_001377131.1:c.1855-35_1855-29del	NP_001364060.1:n.1855-35_1855-29del
NM_001377132.1:c.2578-35_2578-29del	NP_001364061.1:n.2578-35_2578-29del
NM_004036.5:c.2578-35_2578-29del MANE Select	NP_004027.2:n.2578-35_2578-29del