Canonical Allele Identifier: CA346062723

Gene: ADCY3

Linked Data

• gnomAD v4: 2-24823273-C-G
• MyVariant Identifiers: chr2:g.25046142C>G (hg19) ; chr2:g.24823273C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823273C>G , CM000664.2:g.24823273C>G	GRCh38
NC_000002.11:g.25046142C>G , CM000664.1:g.25046142C>G	GRCh37
NC_000002.10:g.24899646C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2822G>C	ENSP00000384484.2:p.Ser941Thr
ENST00000679454.1:c.2819G>C MANE Select	ENSP00000505261.1:p.Ser940Thr
ENST00000260600.9:c.2819G>C	ENSP00000260600.5:p.Ser940Thr
ENST00000405392.5:c.2822G>C	ENSP00000384484.2:p.Ser941Thr
ENST00000485887.1:n.91G>C
ENST00000606682.5:c.1760G>C	ENSP00000475652.1:p.Ser587Thr
NM_004036.3:c.2819G>C	NP_004027.2:p.Ser940Thr
XM_005264104.1:c.2822G>C	XP_005264161.1:p.Ser941Thr
XM_005264105.1:c.2819G>C	XP_005264162.1:p.Ser940Thr
XM_006711925.1:c.2888G>C	XP_006711988.1:p.Ser963Thr
XM_011532489.1:c.2945G>C	XP_011530791.1:p.Ser982Thr
XM_011532490.1:c.2942G>C	XP_011530792.1:p.Ser981Thr
XM_011532491.1:c.2879G>C	XP_011530793.1:p.Ser960Thr
XM_011532492.1:c.2945G>C	XP_011530794.1:p.Ser982Thr
XM_011532493.1:c.2807G>C	XP_011530795.1:p.Ser936Thr
XM_011532494.1:c.2747G>C	XP_011530796.1:p.Ser916Thr
XM_011532495.1:c.2279G>C	XP_011530797.1:p.Ser760Thr
XM_011532496.1:c.2222G>C	XP_011530798.1:p.Ser741Thr
NM_001320613.1:c.2822G>C	NP_001307542.1:p.Ser941Thr
NM_004036.4:c.2819G>C	NP_004027.2:p.Ser940Thr
XM_011532492.2:c.2945G>C	XP_011530794.1:p.Ser982Thr
XM_017003186.1:c.2885G>C	XP_016858675.1:p.Ser962Thr
XM_017003187.1:c.2876G>C	XP_016858676.1:p.Ser959Thr
XM_017003188.1:c.2942G>C	XP_016858677.1:p.Ser981Thr
XM_017003189.1:c.2804G>C	XP_016858678.1:p.Ser935Thr
XM_017003190.1:c.2681G>C	XP_016858679.1:p.Ser894Thr
XM_017003191.1:c.2309G>C	XP_016858680.1:p.Ser770Thr
XM_017003192.1:c.2099G>C	XP_016858681.1:p.Ser700Thr
XM_017003193.1:c.2096G>C	XP_016858682.1:p.Ser699Thr
NM_001320613.2:c.2822G>C	NP_001307542.1:p.Ser941Thr
NM_001377128.1:c.2885G>C	NP_001364057.1:p.Ser962Thr
NM_001377129.1:c.2681G>C	NP_001364058.1:p.Ser894Thr
NM_001377130.1:c.2332-643G>C	NP_001364059.1:n.2332-643G>C
NM_001377131.1:c.2096G>C	NP_001364060.1:p.Ser699Thr
NM_001377132.1:c.2819G>C	NP_001364061.1:p.Ser940Thr
NM_004036.5:c.2819G>C MANE Select	NP_004027.2:p.Ser940Thr