Canonical Allele Identifier: CA1553651

Gene: ADCY3

Linked Data

• ClinVar Variation Id: 3038767
• ClinVar RCV Id: RCV003922168
• dbSNP Id: rs199524620
• ExAC: 2:25047327 G / A
• gnomAD v2: 2-25047327-G-A
• gnomAD v3: 2-24824458-G-A
• gnomAD v4: 2-24824458-G-A
• MyVariant Identifiers: chr2:g.25047327G>A (hg19) ; chr2:g.24824458G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824458G>A , CM000664.2:g.24824458G>A	GRCh38
NC_000002.11:g.25047327G>A , CM000664.1:g.25047327G>A	GRCh37
NC_000002.10:g.24900831G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2659C>T	ENSP00000384484.2:p.Arg887Cys
ENST00000679454.1:c.2656C>T MANE Select	ENSP00000505261.1:p.Arg886Cys
ENST00000260600.9:c.2656C>T	ENSP00000260600.5:p.Arg886Cys
ENST00000405392.5:c.2659C>T	ENSP00000384484.2:p.Arg887Cys
ENST00000606682.5:c.1597C>T	ENSP00000475652.1:p.Arg533Cys
NM_004036.3:c.2656C>T	NP_004027.2:p.Arg886Cys
XM_005264104.1:c.2659C>T	XP_005264161.1:p.Arg887Cys
XM_005264105.1:c.2656C>T	XP_005264162.1:p.Arg886Cys
XM_006711925.1:c.2725C>T	XP_006711988.1:p.Arg909Cys
XM_011532489.1:c.2782C>T	XP_011530791.1:p.Arg928Cys
XM_011532490.1:c.2779C>T	XP_011530792.1:p.Arg927Cys
XM_011532491.1:c.2716C>T	XP_011530793.1:p.Arg906Cys
XM_011532492.1:c.2782C>T	XP_011530794.1:p.Arg928Cys
XM_011532493.1:c.2644C>T	XP_011530795.1:p.Arg882Cys
XM_011532494.1:c.2584C>T	XP_011530796.1:p.Arg862Cys
XM_011532495.1:c.2116C>T	XP_011530797.1:p.Arg706Cys
XM_011532496.1:c.2059C>T	XP_011530798.1:p.Arg687Cys
NM_001320613.1:c.2659C>T	NP_001307542.1:p.Arg887Cys
NM_004036.4:c.2656C>T	NP_004027.2:p.Arg886Cys
XM_011532492.2:c.2782C>T	XP_011530794.1:p.Arg928Cys
XM_017003186.1:c.2722C>T	XP_016858675.1:p.Arg908Cys
XM_017003187.1:c.2713C>T	XP_016858676.1:p.Arg905Cys
XM_017003188.1:c.2779C>T	XP_016858677.1:p.Arg927Cys
XM_017003189.1:c.2641C>T	XP_016858678.1:p.Arg881Cys
XM_017003190.1:c.2518C>T	XP_016858679.1:p.Arg840Cys
XM_017003191.1:c.2146C>T	XP_016858680.1:p.Arg716Cys
XM_017003192.1:c.1936C>T	XP_016858681.1:p.Arg646Cys
XM_017003193.1:c.1933C>T	XP_016858682.1:p.Arg645Cys
NM_001320613.2:c.2659C>T	NP_001307542.1:p.Arg887Cys
NM_001377128.1:c.2722C>T	NP_001364057.1:p.Arg908Cys
NM_001377129.1:c.2518C>T	NP_001364058.1:p.Arg840Cys
NM_001377130.1:c.2251C>T	NP_001364059.1:p.Arg751Cys
NM_001377131.1:c.1933C>T	NP_001364060.1:p.Arg645Cys
NM_001377132.1:c.2656C>T	NP_001364061.1:p.Arg886Cys
NM_004036.5:c.2656C>T MANE Select	NP_004027.2:p.Arg886Cys