Canonical Allele Identifier: CA346063604
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24824442A>T , CM000664.2:g.24824442A>T GRCh38
NC_000002.11:g.25047311A>T , CM000664.1:g.25047311A>T GRCh37
NC_000002.10:g.24900815A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000405392.6:c.2675T>A ENSP00000384484.2:p.Leu892Ter
ENST00000679454.1:c.2672T>A MANE Select ENSP00000505261.1:p.Leu891Ter
ENST00000260600.9:c.2672T>A ENSP00000260600.5:p.Leu891Ter
ENST00000405392.5:c.2675T>A ENSP00000384484.2:p.Leu892Ter
ENST00000606682.5:c.1613T>A ENSP00000475652.1:p.Leu538Ter
NM_004036.3:c.2672T>A NP_004027.2:p.Leu891Ter
XM_005264104.1:c.2675T>A XP_005264161.1:p.Leu892Ter
XM_005264105.1:c.2672T>A XP_005264162.1:p.Leu891Ter
XM_006711925.1:c.2741T>A XP_006711988.1:p.Leu914Ter
XM_011532489.1:c.2798T>A XP_011530791.1:p.Leu933Ter
XM_011532490.1:c.2795T>A XP_011530792.1:p.Leu932Ter
XM_011532491.1:c.2732T>A XP_011530793.1:p.Leu911Ter
XM_011532492.1:c.2798T>A XP_011530794.1:p.Leu933Ter
XM_011532493.1:c.2660T>A XP_011530795.1:p.Leu887Ter
XM_011532494.1:c.2600T>A XP_011530796.1:p.Leu867Ter
XM_011532495.1:c.2132T>A XP_011530797.1:p.Leu711Ter
XM_011532496.1:c.2075T>A XP_011530798.1:p.Leu692Ter
NM_001320613.1:c.2675T>A NP_001307542.1:p.Leu892Ter
NM_004036.4:c.2672T>A NP_004027.2:p.Leu891Ter
XM_011532492.2:c.2798T>A XP_011530794.1:p.Leu933Ter
XM_017003186.1:c.2738T>A XP_016858675.1:p.Leu913Ter
XM_017003187.1:c.2729T>A XP_016858676.1:p.Leu910Ter
XM_017003188.1:c.2795T>A XP_016858677.1:p.Leu932Ter
XM_017003189.1:c.2657T>A XP_016858678.1:p.Leu886Ter
XM_017003190.1:c.2534T>A XP_016858679.1:p.Leu845Ter
XM_017003191.1:c.2162T>A XP_016858680.1:p.Leu721Ter
XM_017003192.1:c.1952T>A XP_016858681.1:p.Leu651Ter
XM_017003193.1:c.1949T>A XP_016858682.1:p.Leu650Ter
NM_001320613.2:c.2675T>A NP_001307542.1:p.Leu892Ter
NM_001377128.1:c.2738T>A NP_001364057.1:p.Leu913Ter
NM_001377129.1:c.2534T>A NP_001364058.1:p.Leu845Ter
NM_001377130.1:c.2267T>A NP_001364059.1:p.Leu756Ter
NM_001377131.1:c.1949T>A NP_001364060.1:p.Leu650Ter
NM_001377132.1:c.2672T>A NP_001364061.1:p.Leu891Ter
NM_004036.5:c.2672T>A MANE Select NP_004027.2:p.Leu891Ter