Canonical Allele Identifier: CA346062879

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046167A>T (hg19) ; chr2:g.24823298A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823298A>T , CM000664.2:g.24823298A>T	GRCh38
NC_000002.11:g.25046167A>T , CM000664.1:g.25046167A>T	GRCh37
NC_000002.10:g.24899671A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2797T>A	ENSP00000384484.2:p.Phe933Ile
ENST00000679454.1:c.2794T>A MANE Select	ENSP00000505261.1:p.Phe932Ile
ENST00000260600.9:c.2794T>A	ENSP00000260600.5:p.Phe932Ile
ENST00000405392.5:c.2797T>A	ENSP00000384484.2:p.Phe933Ile
ENST00000485887.1:n.66T>A
ENST00000606682.5:c.1735T>A	ENSP00000475652.1:p.Phe579Ile
NM_004036.3:c.2794T>A	NP_004027.2:p.Phe932Ile
XM_005264104.1:c.2797T>A	XP_005264161.1:p.Phe933Ile
XM_005264105.1:c.2794T>A	XP_005264162.1:p.Phe932Ile
XM_006711925.1:c.2863T>A	XP_006711988.1:p.Phe955Ile
XM_011532489.1:c.2920T>A	XP_011530791.1:p.Phe974Ile
XM_011532490.1:c.2917T>A	XP_011530792.1:p.Phe973Ile
XM_011532491.1:c.2854T>A	XP_011530793.1:p.Phe952Ile
XM_011532492.1:c.2920T>A	XP_011530794.1:p.Phe974Ile
XM_011532493.1:c.2782T>A	XP_011530795.1:p.Phe928Ile
XM_011532494.1:c.2722T>A	XP_011530796.1:p.Phe908Ile
XM_011532495.1:c.2254T>A	XP_011530797.1:p.Phe752Ile
XM_011532496.1:c.2197T>A	XP_011530798.1:p.Phe733Ile
NM_001320613.1:c.2797T>A	NP_001307542.1:p.Phe933Ile
NM_004036.4:c.2794T>A	NP_004027.2:p.Phe932Ile
XM_011532492.2:c.2920T>A	XP_011530794.1:p.Phe974Ile
XM_017003186.1:c.2860T>A	XP_016858675.1:p.Phe954Ile
XM_017003187.1:c.2851T>A	XP_016858676.1:p.Phe951Ile
XM_017003188.1:c.2917T>A	XP_016858677.1:p.Phe973Ile
XM_017003189.1:c.2779T>A	XP_016858678.1:p.Phe927Ile
XM_017003190.1:c.2656T>A	XP_016858679.1:p.Phe886Ile
XM_017003191.1:c.2284T>A	XP_016858680.1:p.Phe762Ile
XM_017003192.1:c.2074T>A	XP_016858681.1:p.Phe692Ile
XM_017003193.1:c.2071T>A	XP_016858682.1:p.Phe691Ile
NM_001320613.2:c.2797T>A	NP_001307542.1:p.Phe933Ile
NM_001377128.1:c.2860T>A	NP_001364057.1:p.Phe954Ile
NM_001377129.1:c.2656T>A	NP_001364058.1:p.Phe886Ile
NM_001377130.1:c.2332-668T>A	NP_001364059.1:n.2332-668T>A
NM_001377131.1:c.2071T>A	NP_001364060.1:p.Phe691Ile
NM_001377132.1:c.2794T>A	NP_001364061.1:p.Phe932Ile
NM_004036.5:c.2794T>A MANE Select	NP_004027.2:p.Phe932Ile