Canonical Allele Identifier: CA425171987

Gene: ADCY3

Linked Data

• dbSNP Id: rs1668054627
• MyVariant Identifiers: chr2:g.25046138G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823269G>A , CM000664.2:g.24823269G>A	GRCh38
NC_000002.11:g.25046138G>A , CM000664.1:g.25046138G>A	GRCh37
NC_000002.10:g.24899642G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2826C>T	ENSP00000384484.2:p.Ile942=
ENST00000679454.1:c.2823C>T MANE Select	ENSP00000505261.1:p.Ile941=
ENST00000260600.9:c.2823C>T	ENSP00000260600.5:p.Ile941=
ENST00000405392.5:c.2826C>T	ENSP00000384484.2:p.Ile942=
ENST00000485887.1:n.95C>T
ENST00000606682.5:c.1764C>T	ENSP00000475652.1:p.Ile588=
NM_004036.3:c.2823C>T	NP_004027.2:p.Ile941=
XM_005264104.1:c.2826C>T	XP_005264161.1:p.Ile942=
XM_005264105.1:c.2823C>T	XP_005264162.1:p.Ile941=
XM_006711925.1:c.2892C>T	XP_006711988.1:p.Ile964=
XM_011532489.1:c.2949C>T	XP_011530791.1:p.Ile983=
XM_011532490.1:c.2946C>T	XP_011530792.1:p.Ile982=
XM_011532491.1:c.2883C>T	XP_011530793.1:p.Ile961=
XM_011532492.1:c.2949C>T	XP_011530794.1:p.Ile983=
XM_011532493.1:c.2811C>T	XP_011530795.1:p.Ile937=
XM_011532494.1:c.2751C>T	XP_011530796.1:p.Ile917=
XM_011532495.1:c.2283C>T	XP_011530797.1:p.Ile761=
XM_011532496.1:c.2226C>T	XP_011530798.1:p.Ile742=
NM_001320613.1:c.2826C>T	NP_001307542.1:p.Ile942=
NM_004036.4:c.2823C>T	NP_004027.2:p.Ile941=
XM_011532492.2:c.2949C>T	XP_011530794.1:p.Ile983=
XM_017003186.1:c.2889C>T	XP_016858675.1:p.Ile963=
XM_017003187.1:c.2880C>T	XP_016858676.1:p.Ile960=
XM_017003188.1:c.2946C>T	XP_016858677.1:p.Ile982=
XM_017003189.1:c.2808C>T	XP_016858678.1:p.Ile936=
XM_017003190.1:c.2685C>T	XP_016858679.1:p.Ile895=
XM_017003191.1:c.2313C>T	XP_016858680.1:p.Ile771=
XM_017003192.1:c.2103C>T	XP_016858681.1:p.Ile701=
XM_017003193.1:c.2100C>T	XP_016858682.1:p.Ile700=
NM_001320613.2:c.2826C>T	NP_001307542.1:p.Ile942=
NM_001377128.1:c.2889C>T	NP_001364057.1:p.Ile963=
NM_001377129.1:c.2685C>T	NP_001364058.1:p.Ile895=
NM_001377130.1:c.2332-639C>T	NP_001364059.1:n.2332-639C>T
NM_001377131.1:c.2100C>T	NP_001364060.1:p.Ile700=
NM_001377132.1:c.2823C>T	NP_001364061.1:p.Ile941=
NM_004036.5:c.2823C>T MANE Select	NP_004027.2:p.Ile941=