Canonical Allele Identifier: CA1554559
Gene: ADCY3 HGNC NCBI

Linked Data

dbSNP Id: rs541941351

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24918797T>A , CM000664.2:g.24918797T>A GRCh38
NC_000002.11:g.25141666T>A , CM000664.1:g.25141666T>A GRCh37
NC_000002.10:g.24995170T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260600.9:c.191A>T ENSP00000260600.5:p.Asn64Ile
ENST00000405392.5:c.191A>T ENSP00000384484.2:p.Asn64Ile
ENST00000435135.5:c.191A>T ENSP00000389799.1:p.Asn64Ile
ENST00000438445.1:c.191A>T ENSP00000406153.1:p.Asn64Ile
NM_004036.3:c.191A>T NP_004027.2:p.Asn64Ile
XM_005264104.1:c.191A>T XP_005264161.1:p.Asn64Ile
XM_005264105.1:c.191A>T XP_005264162.1:p.Asn64Ile
XM_006711925.1:c.191A>T XP_006711988.1:p.Asn64Ile
XM_011532489.1:c.191A>T XP_011530791.1:p.Asn64Ile
XM_011532490.1:c.191A>T XP_011530792.1:p.Asn64Ile
XM_011532491.1:c.191A>T XP_011530793.1:p.Asn64Ile
XM_011532492.1:c.191A>T XP_011530794.1:p.Asn64Ile
XM_011532493.1:c.191A>T XP_011530795.1:p.Asn64Ile
XM_011532494.1:c.191A>T XP_011530796.1:p.Asn64Ile
NM_001320613.1:c.191A>T NP_001307542.1:p.Asn64Ile
NM_004036.4:c.191A>T NP_004027.2:p.Asn64Ile
XM_011532492.2:c.191A>T XP_011530794.1:p.Asn64Ile
XM_017003186.1:c.191A>T XP_016858675.1:p.Asn64Ile
XM_017003187.1:c.191A>T XP_016858676.1:p.Asn64Ile
XM_017003188.1:c.191A>T XP_016858677.1:p.Asn64Ile
XM_017003189.1:c.191A>T XP_016858678.1:p.Asn64Ile
XM_017003190.1:c.191A>T XP_016858679.1:p.Asn64Ile
NM_001320613.2:c.191A>T NP_001307542.1:p.Asn64Ile
NM_001377128.1:c.191A>T NP_001364057.1:p.Asn64Ile
NM_001377129.1:c.191A>T NP_001364058.1:p.Asn64Ile
NM_001377130.1:c.191A>T NP_001364059.1:p.Asn64Ile
NM_001377132.1:c.191A>T NP_001364061.1:p.Asn64Ile
NM_004036.5:c.191A>T MANE Select NP_004027.2:p.Asn64Ile