Canonical Allele Identifier: CA346062967
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823318A>T , CM000664.2:g.24823318A>T GRCh38
NC_000002.11:g.25046187A>T , CM000664.1:g.25046187A>T GRCh37
NC_000002.10:g.24899691A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2777T>A ENSP00000384484.2:p.Met926Lys
ENST00000679454.1:c.2774T>A MANE Select ENSP00000505261.1:p.Met925Lys
ENST00000260600.9:c.2774T>A ENSP00000260600.5:p.Met925Lys
ENST00000405392.5:c.2777T>A ENSP00000384484.2:p.Met926Lys
ENST00000485887.1:n.46T>A
ENST00000606682.5:c.1715T>A ENSP00000475652.1:p.Met572Lys
NM_004036.3:c.2774T>A NP_004027.2:p.Met925Lys
XM_005264104.1:c.2777T>A XP_005264161.1:p.Met926Lys
XM_005264105.1:c.2774T>A XP_005264162.1:p.Met925Lys
XM_006711925.1:c.2843T>A XP_006711988.1:p.Met948Lys
XM_011532489.1:c.2900T>A XP_011530791.1:p.Met967Lys
XM_011532490.1:c.2897T>A XP_011530792.1:p.Met966Lys
XM_011532491.1:c.2834T>A XP_011530793.1:p.Met945Lys
XM_011532492.1:c.2900T>A XP_011530794.1:p.Met967Lys
XM_011532493.1:c.2762T>A XP_011530795.1:p.Met921Lys
XM_011532494.1:c.2702T>A XP_011530796.1:p.Met901Lys
XM_011532495.1:c.2234T>A XP_011530797.1:p.Met745Lys
XM_011532496.1:c.2177T>A XP_011530798.1:p.Met726Lys
NM_001320613.1:c.2777T>A NP_001307542.1:p.Met926Lys
NM_004036.4:c.2774T>A NP_004027.2:p.Met925Lys
XM_011532492.2:c.2900T>A XP_011530794.1:p.Met967Lys
XM_017003186.1:c.2840T>A XP_016858675.1:p.Met947Lys
XM_017003187.1:c.2831T>A XP_016858676.1:p.Met944Lys
XM_017003188.1:c.2897T>A XP_016858677.1:p.Met966Lys
XM_017003189.1:c.2759T>A XP_016858678.1:p.Met920Lys
XM_017003190.1:c.2636T>A XP_016858679.1:p.Met879Lys
XM_017003191.1:c.2264T>A XP_016858680.1:p.Met755Lys
XM_017003192.1:c.2054T>A XP_016858681.1:p.Met685Lys
XM_017003193.1:c.2051T>A XP_016858682.1:p.Met684Lys
NM_001320613.2:c.2777T>A NP_001307542.1:p.Met926Lys
NM_001377128.1:c.2840T>A NP_001364057.1:p.Met947Lys
NM_001377129.1:c.2636T>A NP_001364058.1:p.Met879Lys
NM_001377130.1:c.2332-688T>A NP_001364059.1:n.2332-688T>A
NM_001377131.1:c.2051T>A NP_001364060.1:p.Met684Lys
NM_001377132.1:c.2774T>A NP_001364061.1:p.Met925Lys
NM_004036.5:c.2774T>A MANE Select NP_004027.2:p.Met925Lys