Canonical Allele Identifier: CA346063603
Gene: ADCY3 HGNC NCBI

Linked Data

gnomAD v4: 2-24824442-A-G

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000405392.6:c.2675T>C ENSP00000384484.2:p.Leu892Ser
ENST00000679454.1:c.2672T>C MANE Select ENSP00000505261.1:p.Leu891Ser
ENST00000260600.9:c.2672T>C ENSP00000260600.5:p.Leu891Ser
ENST00000405392.5:c.2675T>C ENSP00000384484.2:p.Leu892Ser
ENST00000606682.5:c.1613T>C ENSP00000475652.1:p.Leu538Ser
NM_004036.3:c.2672T>C NP_004027.2:p.Leu891Ser
XM_005264104.1:c.2675T>C XP_005264161.1:p.Leu892Ser
XM_005264105.1:c.2672T>C XP_005264162.1:p.Leu891Ser
XM_006711925.1:c.2741T>C XP_006711988.1:p.Leu914Ser
XM_011532489.1:c.2798T>C XP_011530791.1:p.Leu933Ser
XM_011532490.1:c.2795T>C XP_011530792.1:p.Leu932Ser
XM_011532491.1:c.2732T>C XP_011530793.1:p.Leu911Ser
XM_011532492.1:c.2798T>C XP_011530794.1:p.Leu933Ser
XM_011532493.1:c.2660T>C XP_011530795.1:p.Leu887Ser
XM_011532494.1:c.2600T>C XP_011530796.1:p.Leu867Ser
XM_011532495.1:c.2132T>C XP_011530797.1:p.Leu711Ser
XM_011532496.1:c.2075T>C XP_011530798.1:p.Leu692Ser
NM_001320613.1:c.2675T>C NP_001307542.1:p.Leu892Ser
NM_004036.4:c.2672T>C NP_004027.2:p.Leu891Ser
XM_011532492.2:c.2798T>C XP_011530794.1:p.Leu933Ser
XM_017003186.1:c.2738T>C XP_016858675.1:p.Leu913Ser
XM_017003187.1:c.2729T>C XP_016858676.1:p.Leu910Ser
XM_017003188.1:c.2795T>C XP_016858677.1:p.Leu932Ser
XM_017003189.1:c.2657T>C XP_016858678.1:p.Leu886Ser
XM_017003190.1:c.2534T>C XP_016858679.1:p.Leu845Ser
XM_017003191.1:c.2162T>C XP_016858680.1:p.Leu721Ser
XM_017003192.1:c.1952T>C XP_016858681.1:p.Leu651Ser
XM_017003193.1:c.1949T>C XP_016858682.1:p.Leu650Ser
NM_001320613.2:c.2675T>C NP_001307542.1:p.Leu892Ser
NM_001377128.1:c.2738T>C NP_001364057.1:p.Leu913Ser
NM_001377129.1:c.2534T>C NP_001364058.1:p.Leu845Ser
NM_001377130.1:c.2267T>C NP_001364059.1:p.Leu756Ser
NM_001377131.1:c.1949T>C NP_001364060.1:p.Leu650Ser
NM_001377132.1:c.2672T>C NP_001364061.1:p.Leu891Ser
NM_004036.5:c.2672T>C MANE Select NP_004027.2:p.Leu891Ser