Canonical Allele Identifier: CA346062555

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046110A>T (hg19) ; chr2:g.24823241A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823241A>T , CM000664.2:g.24823241A>T	GRCh38
NC_000002.11:g.25046110A>T , CM000664.1:g.25046110A>T	GRCh37
NC_000002.10:g.24899614A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2854T>A	ENSP00000384484.2:p.Phe952Ile
ENST00000679454.1:c.2851T>A MANE Select	ENSP00000505261.1:p.Phe951Ile
ENST00000260600.9:c.2851T>A	ENSP00000260600.5:p.Phe951Ile
ENST00000405392.5:c.2854T>A	ENSP00000384484.2:p.Phe952Ile
ENST00000485887.1:n.123T>A
ENST00000606682.5:c.1792T>A	ENSP00000475652.1:p.Phe598Ile
NM_004036.3:c.2851T>A	NP_004027.2:p.Phe951Ile
XM_005264104.1:c.2854T>A	XP_005264161.1:p.Phe952Ile
XM_005264105.1:c.2851T>A	XP_005264162.1:p.Phe951Ile
XM_006711925.1:c.2920T>A	XP_006711988.1:p.Phe974Ile
XM_011532489.1:c.2977T>A	XP_011530791.1:p.Phe993Ile
XM_011532490.1:c.2974T>A	XP_011530792.1:p.Phe992Ile
XM_011532491.1:c.2911T>A	XP_011530793.1:p.Phe971Ile
XM_011532492.1:c.2977T>A	XP_011530794.1:p.Phe993Ile
XM_011532493.1:c.2839T>A	XP_011530795.1:p.Phe947Ile
XM_011532494.1:c.2779T>A	XP_011530796.1:p.Phe927Ile
XM_011532495.1:c.2311T>A	XP_011530797.1:p.Phe771Ile
XM_011532496.1:c.2254T>A	XP_011530798.1:p.Phe752Ile
NM_001320613.1:c.2854T>A	NP_001307542.1:p.Phe952Ile
NM_004036.4:c.2851T>A	NP_004027.2:p.Phe951Ile
XM_011532492.2:c.2977T>A	XP_011530794.1:p.Phe993Ile
XM_017003186.1:c.2917T>A	XP_016858675.1:p.Phe973Ile
XM_017003187.1:c.2908T>A	XP_016858676.1:p.Phe970Ile
XM_017003188.1:c.2974T>A	XP_016858677.1:p.Phe992Ile
XM_017003189.1:c.2836T>A	XP_016858678.1:p.Phe946Ile
XM_017003190.1:c.2713T>A	XP_016858679.1:p.Phe905Ile
XM_017003191.1:c.2341T>A	XP_016858680.1:p.Phe781Ile
XM_017003192.1:c.2131T>A	XP_016858681.1:p.Phe711Ile
XM_017003193.1:c.2128T>A	XP_016858682.1:p.Phe710Ile
NM_001320613.2:c.2854T>A	NP_001307542.1:p.Phe952Ile
NM_001377128.1:c.2917T>A	NP_001364057.1:p.Phe973Ile
NM_001377129.1:c.2713T>A	NP_001364058.1:p.Phe905Ile
NM_001377130.1:c.2332-611T>A	NP_001364059.1:n.2332-611T>A
NM_001377131.1:c.2128T>A	NP_001364060.1:p.Phe710Ile
NM_001377132.1:c.2851T>A	NP_001364061.1:p.Phe951Ile
NM_004036.5:c.2851T>A MANE Select	NP_004027.2:p.Phe951Ile