Canonical Allele Identifier: CA346063626
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24824450G>T , CM000664.2:g.24824450G>T GRCh38
NC_000002.11:g.25047319G>T , CM000664.1:g.25047319G>T GRCh37
NC_000002.10:g.24900823G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000405392.6:c.2667C>A ENSP00000384484.2:p.Asn889Lys
ENST00000679454.1:c.2664C>A MANE Select ENSP00000505261.1:p.Asn888Lys
ENST00000260600.9:c.2664C>A ENSP00000260600.5:p.Asn888Lys
ENST00000405392.5:c.2667C>A ENSP00000384484.2:p.Asn889Lys
ENST00000606682.5:c.1605C>A ENSP00000475652.1:p.Asn535Lys
NM_004036.3:c.2664C>A NP_004027.2:p.Asn888Lys
XM_005264104.1:c.2667C>A XP_005264161.1:p.Asn889Lys
XM_005264105.1:c.2664C>A XP_005264162.1:p.Asn888Lys
XM_006711925.1:c.2733C>A XP_006711988.1:p.Asn911Lys
XM_011532489.1:c.2790C>A XP_011530791.1:p.Asn930Lys
XM_011532490.1:c.2787C>A XP_011530792.1:p.Asn929Lys
XM_011532491.1:c.2724C>A XP_011530793.1:p.Asn908Lys
XM_011532492.1:c.2790C>A XP_011530794.1:p.Asn930Lys
XM_011532493.1:c.2652C>A XP_011530795.1:p.Asn884Lys
XM_011532494.1:c.2592C>A XP_011530796.1:p.Asn864Lys
XM_011532495.1:c.2124C>A XP_011530797.1:p.Asn708Lys
XM_011532496.1:c.2067C>A XP_011530798.1:p.Asn689Lys
NM_001320613.1:c.2667C>A NP_001307542.1:p.Asn889Lys
NM_004036.4:c.2664C>A NP_004027.2:p.Asn888Lys
XM_011532492.2:c.2790C>A XP_011530794.1:p.Asn930Lys
XM_017003186.1:c.2730C>A XP_016858675.1:p.Asn910Lys
XM_017003187.1:c.2721C>A XP_016858676.1:p.Asn907Lys
XM_017003188.1:c.2787C>A XP_016858677.1:p.Asn929Lys
XM_017003189.1:c.2649C>A XP_016858678.1:p.Asn883Lys
XM_017003190.1:c.2526C>A XP_016858679.1:p.Asn842Lys
XM_017003191.1:c.2154C>A XP_016858680.1:p.Asn718Lys
XM_017003192.1:c.1944C>A XP_016858681.1:p.Asn648Lys
XM_017003193.1:c.1941C>A XP_016858682.1:p.Asn647Lys
NM_001320613.2:c.2667C>A NP_001307542.1:p.Asn889Lys
NM_001377128.1:c.2730C>A NP_001364057.1:p.Asn910Lys
NM_001377129.1:c.2526C>A NP_001364058.1:p.Asn842Lys
NM_001377130.1:c.2259C>A NP_001364059.1:p.Asn753Lys
NM_001377131.1:c.1941C>A NP_001364060.1:p.Asn647Lys
NM_001377132.1:c.2664C>A NP_001364061.1:p.Asn888Lys
NM_004036.5:c.2664C>A MANE Select NP_004027.2:p.Asn888Lys