Canonical Allele Identifier: CA346062992

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046197T>A (hg19) ; chr2:g.24823328T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823328T>A , CM000664.2:g.24823328T>A	GRCh38
NC_000002.11:g.25046197T>A , CM000664.1:g.25046197T>A	GRCh37
NC_000002.10:g.24899701T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2767A>T	ENSP00000384484.2:p.Ile923Phe
ENST00000679454.1:c.2764A>T MANE Select	ENSP00000505261.1:p.Ile922Phe
ENST00000260600.9:c.2764A>T	ENSP00000260600.5:p.Ile922Phe
ENST00000405392.5:c.2767A>T	ENSP00000384484.2:p.Ile923Phe
ENST00000485887.1:n.36A>T
ENST00000606682.5:c.1705A>T	ENSP00000475652.1:p.Ile569Phe
NM_004036.3:c.2764A>T	NP_004027.2:p.Ile922Phe
XM_005264104.1:c.2767A>T	XP_005264161.1:p.Ile923Phe
XM_005264105.1:c.2764A>T	XP_005264162.1:p.Ile922Phe
XM_006711925.1:c.2833A>T	XP_006711988.1:p.Ile945Phe
XM_011532489.1:c.2890A>T	XP_011530791.1:p.Ile964Phe
XM_011532490.1:c.2887A>T	XP_011530792.1:p.Ile963Phe
XM_011532491.1:c.2824A>T	XP_011530793.1:p.Ile942Phe
XM_011532492.1:c.2890A>T	XP_011530794.1:p.Ile964Phe
XM_011532493.1:c.2752A>T	XP_011530795.1:p.Ile918Phe
XM_011532494.1:c.2692A>T	XP_011530796.1:p.Ile898Phe
XM_011532495.1:c.2224A>T	XP_011530797.1:p.Ile742Phe
XM_011532496.1:c.2167A>T	XP_011530798.1:p.Ile723Phe
NM_001320613.1:c.2767A>T	NP_001307542.1:p.Ile923Phe
NM_004036.4:c.2764A>T	NP_004027.2:p.Ile922Phe
XM_011532492.2:c.2890A>T	XP_011530794.1:p.Ile964Phe
XM_017003186.1:c.2830A>T	XP_016858675.1:p.Ile944Phe
XM_017003187.1:c.2821A>T	XP_016858676.1:p.Ile941Phe
XM_017003188.1:c.2887A>T	XP_016858677.1:p.Ile963Phe
XM_017003189.1:c.2749A>T	XP_016858678.1:p.Ile917Phe
XM_017003190.1:c.2626A>T	XP_016858679.1:p.Ile876Phe
XM_017003191.1:c.2254A>T	XP_016858680.1:p.Ile752Phe
XM_017003192.1:c.2044A>T	XP_016858681.1:p.Ile682Phe
XM_017003193.1:c.2041A>T	XP_016858682.1:p.Ile681Phe
NM_001320613.2:c.2767A>T	NP_001307542.1:p.Ile923Phe
NM_001377128.1:c.2830A>T	NP_001364057.1:p.Ile944Phe
NM_001377129.1:c.2626A>T	NP_001364058.1:p.Ile876Phe
NM_001377130.1:c.2332-698A>T	NP_001364059.1:n.2332-698A>T
NM_001377131.1:c.2041A>T	NP_001364060.1:p.Ile681Phe
NM_001377132.1:c.2764A>T	NP_001364061.1:p.Ile922Phe
NM_004036.5:c.2764A>T MANE Select	NP_004027.2:p.Ile922Phe