Canonical Allele Identifier: CA346062515

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046098T>A (hg19) ; chr2:g.24823229T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823229T>A , CM000664.2:g.24823229T>A	GRCh38
NC_000002.11:g.25046098T>A , CM000664.1:g.25046098T>A	GRCh37
NC_000002.10:g.24899602T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2866A>T	ENSP00000384484.2:p.Ile956Phe
ENST00000679454.1:c.2863A>T MANE Select	ENSP00000505261.1:p.Ile955Phe
ENST00000260600.9:c.2863A>T	ENSP00000260600.5:p.Ile955Phe
ENST00000405392.5:c.2866A>T	ENSP00000384484.2:p.Ile956Phe
ENST00000485887.1:n.135A>T
ENST00000606682.5:c.1804A>T	ENSP00000475652.1:p.Ile602Phe
NM_004036.3:c.2863A>T	NP_004027.2:p.Ile955Phe
XM_005264104.1:c.2866A>T	XP_005264161.1:p.Ile956Phe
XM_005264105.1:c.2863A>T	XP_005264162.1:p.Ile955Phe
XM_006711925.1:c.2932A>T	XP_006711988.1:p.Ile978Phe
XM_011532489.1:c.2989A>T	XP_011530791.1:p.Ile997Phe
XM_011532490.1:c.2986A>T	XP_011530792.1:p.Ile996Phe
XM_011532491.1:c.2923A>T	XP_011530793.1:p.Ile975Phe
XM_011532492.1:c.2989A>T	XP_011530794.1:p.Ile997Phe
XM_011532493.1:c.2851A>T	XP_011530795.1:p.Ile951Phe
XM_011532494.1:c.2791A>T	XP_011530796.1:p.Ile931Phe
XM_011532495.1:c.2323A>T	XP_011530797.1:p.Ile775Phe
XM_011532496.1:c.2266A>T	XP_011530798.1:p.Ile756Phe
NM_001320613.1:c.2866A>T	NP_001307542.1:p.Ile956Phe
NM_004036.4:c.2863A>T	NP_004027.2:p.Ile955Phe
XM_011532492.2:c.2989A>T	XP_011530794.1:p.Ile997Phe
XM_017003186.1:c.2929A>T	XP_016858675.1:p.Ile977Phe
XM_017003187.1:c.2920A>T	XP_016858676.1:p.Ile974Phe
XM_017003188.1:c.2986A>T	XP_016858677.1:p.Ile996Phe
XM_017003189.1:c.2848A>T	XP_016858678.1:p.Ile950Phe
XM_017003190.1:c.2725A>T	XP_016858679.1:p.Ile909Phe
XM_017003191.1:c.2353A>T	XP_016858680.1:p.Ile785Phe
XM_017003192.1:c.2143A>T	XP_016858681.1:p.Ile715Phe
XM_017003193.1:c.2140A>T	XP_016858682.1:p.Ile714Phe
NM_001320613.2:c.2866A>T	NP_001307542.1:p.Ile956Phe
NM_001377128.1:c.2929A>T	NP_001364057.1:p.Ile977Phe
NM_001377129.1:c.2725A>T	NP_001364058.1:p.Ile909Phe
NM_001377130.1:c.2332-599A>T	NP_001364059.1:n.2332-599A>T
NM_001377131.1:c.2140A>T	NP_001364060.1:p.Ile714Phe
NM_001377132.1:c.2863A>T	NP_001364061.1:p.Ile955Phe
NM_004036.5:c.2863A>T MANE Select	NP_004027.2:p.Ile955Phe