Canonical Allele Identifier: CA2658140274
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24824648_24824649insACCC , CM000664.2:g.24824648_24824649insACCC GRCh38
NC_000002.11:g.25047517_25047518insACCC , CM000664.1:g.25047517_25047518insACCC GRCh37
NC_000002.10:g.24901021_24901022insACCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2581-113_2581-112insGGGT ENSP00000384484.2:n.2581-113_2581-112insGGGT
ENST00000679454.1:c.2578-113_2578-112insGGGT MANE Select ENSP00000505261.1:n.2578-113_2578-112insGGGT
ENST00000260600.9:c.2578-113_2578-112insGGGT ENSP00000260600.5:n.2578-113_2578-112insGGGT
ENST00000405392.5:c.2581-113_2581-112insGGGT ENSP00000384484.2:n.2581-113_2581-112insGGGT
ENST00000606682.5:c.1519-113_1519-112insGGGT ENSP00000475652.1:n.1519-113_1519-112insGGGT
NM_004036.3:c.2578-113_2578-112insGGGT NP_004027.2:n.2578-113_2578-112insGGGT
XM_005264104.1:c.2581-113_2581-112insGGGT XP_005264161.1:n.2581-113_2581-112insGGGT
XM_005264105.1:c.2578-113_2578-112insGGGT XP_005264162.1:n.2578-113_2578-112insGGGT
XM_006711925.1:c.2647-113_2647-112insGGGT XP_006711988.1:n.2647-113_2647-112insGGGT
XM_011532489.1:c.2704-113_2704-112insGGGT XP_011530791.1:n.2704-113_2704-112insGGGT
XM_011532490.1:c.2701-113_2701-112insGGGT XP_011530792.1:n.2701-113_2701-112insGGGT
XM_011532491.1:c.2638-113_2638-112insGGGT XP_011530793.1:n.2638-113_2638-112insGGGT
XM_011532492.1:c.2704-113_2704-112insGGGT XP_011530794.1:n.2704-113_2704-112insGGGT
XM_011532493.1:c.2566-113_2566-112insGGGT XP_011530795.1:n.2566-113_2566-112insGGGT
XM_011532494.1:c.2506-113_2506-112insGGGT XP_011530796.1:n.2506-113_2506-112insGGGT
XM_011532495.1:c.2038-113_2038-112insGGGT XP_011530797.1:n.2038-113_2038-112insGGGT
XM_011532496.1:c.1981-113_1981-112insGGGT XP_011530798.1:n.1981-113_1981-112insGGGT
NM_001320613.1:c.2581-113_2581-112insGGGT NP_001307542.1:n.2581-113_2581-112insGGGT
NM_004036.4:c.2578-113_2578-112insGGGT NP_004027.2:n.2578-113_2578-112insGGGT
XM_011532492.2:c.2704-113_2704-112insGGGT XP_011530794.1:n.2704-113_2704-112insGGGT
XM_017003186.1:c.2644-113_2644-112insGGGT XP_016858675.1:n.2644-113_2644-112insGGGT
XM_017003187.1:c.2635-113_2635-112insGGGT XP_016858676.1:n.2635-113_2635-112insGGGT
XM_017003188.1:c.2701-113_2701-112insGGGT XP_016858677.1:n.2701-113_2701-112insGGGT
XM_017003189.1:c.2563-113_2563-112insGGGT XP_016858678.1:n.2563-113_2563-112insGGGT
XM_017003190.1:c.2440-113_2440-112insGGGT XP_016858679.1:n.2440-113_2440-112insGGGT
XM_017003191.1:c.2068-113_2068-112insGGGT XP_016858680.1:n.2068-113_2068-112insGGGT
XM_017003192.1:c.1858-113_1858-112insGGGT XP_016858681.1:n.1858-113_1858-112insGGGT
XM_017003193.1:c.1855-113_1855-112insGGGT XP_016858682.1:n.1855-113_1855-112insGGGT
NM_001320613.2:c.2581-113_2581-112insGGGT NP_001307542.1:n.2581-113_2581-112insGGGT
NM_001377128.1:c.2644-113_2644-112insGGGT NP_001364057.1:n.2644-113_2644-112insGGGT
NM_001377129.1:c.2440-113_2440-112insGGGT NP_001364058.1:n.2440-113_2440-112insGGGT
NM_001377130.1:c.2173-113_2173-112insGGGT NP_001364059.1:n.2173-113_2173-112insGGGT
NM_001377131.1:c.1855-113_1855-112insGGGT NP_001364060.1:n.1855-113_1855-112insGGGT
NM_001377132.1:c.2578-113_2578-112insGGGT NP_001364061.1:n.2578-113_2578-112insGGGT
NM_004036.5:c.2578-113_2578-112insGGGT MANE Select NP_004027.2:n.2578-113_2578-112insGGGT