Canonical Allele Identifier: CA346062620

Gene: ADCY3

Linked Data

• dbSNP Id: rs1407728096
• gnomAD v2: 2-25046124-A-G
• MyVariant Identifiers: chr2:g.25046124A>G (hg19) ; chr2:g.24823255A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823255A>G , CM000664.2:g.24823255A>G	GRCh38
NC_000002.11:g.25046124A>G , CM000664.1:g.25046124A>G	GRCh37
NC_000002.10:g.24899628A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2840T>C	ENSP00000384484.2:p.Ile947Thr
ENST00000679454.1:c.2837T>C MANE Select	ENSP00000505261.1:p.Ile946Thr
ENST00000260600.9:c.2837T>C	ENSP00000260600.5:p.Ile946Thr
ENST00000405392.5:c.2840T>C	ENSP00000384484.2:p.Ile947Thr
ENST00000485887.1:n.109T>C
ENST00000606682.5:c.1778T>C	ENSP00000475652.1:p.Ile593Thr
NM_004036.3:c.2837T>C	NP_004027.2:p.Ile946Thr
XM_005264104.1:c.2840T>C	XP_005264161.1:p.Ile947Thr
XM_005264105.1:c.2837T>C	XP_005264162.1:p.Ile946Thr
XM_006711925.1:c.2906T>C	XP_006711988.1:p.Ile969Thr
XM_011532489.1:c.2963T>C	XP_011530791.1:p.Ile988Thr
XM_011532490.1:c.2960T>C	XP_011530792.1:p.Ile987Thr
XM_011532491.1:c.2897T>C	XP_011530793.1:p.Ile966Thr
XM_011532492.1:c.2963T>C	XP_011530794.1:p.Ile988Thr
XM_011532493.1:c.2825T>C	XP_011530795.1:p.Ile942Thr
XM_011532494.1:c.2765T>C	XP_011530796.1:p.Ile922Thr
XM_011532495.1:c.2297T>C	XP_011530797.1:p.Ile766Thr
XM_011532496.1:c.2240T>C	XP_011530798.1:p.Ile747Thr
NM_001320613.1:c.2840T>C	NP_001307542.1:p.Ile947Thr
NM_004036.4:c.2837T>C	NP_004027.2:p.Ile946Thr
XM_011532492.2:c.2963T>C	XP_011530794.1:p.Ile988Thr
XM_017003186.1:c.2903T>C	XP_016858675.1:p.Ile968Thr
XM_017003187.1:c.2894T>C	XP_016858676.1:p.Ile965Thr
XM_017003188.1:c.2960T>C	XP_016858677.1:p.Ile987Thr
XM_017003189.1:c.2822T>C	XP_016858678.1:p.Ile941Thr
XM_017003190.1:c.2699T>C	XP_016858679.1:p.Ile900Thr
XM_017003191.1:c.2327T>C	XP_016858680.1:p.Ile776Thr
XM_017003192.1:c.2117T>C	XP_016858681.1:p.Ile706Thr
XM_017003193.1:c.2114T>C	XP_016858682.1:p.Ile705Thr
NM_001320613.2:c.2840T>C	NP_001307542.1:p.Ile947Thr
NM_001377128.1:c.2903T>C	NP_001364057.1:p.Ile968Thr
NM_001377129.1:c.2699T>C	NP_001364058.1:p.Ile900Thr
NM_001377130.1:c.2332-625T>C	NP_001364059.1:n.2332-625T>C
NM_001377131.1:c.2114T>C	NP_001364060.1:p.Ile705Thr
NM_001377132.1:c.2837T>C	NP_001364061.1:p.Ile946Thr
NM_004036.5:c.2837T>C MANE Select	NP_004027.2:p.Ile946Thr