Canonical Allele Identifier: CA346062797

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046152T>A (hg19) ; chr2:g.24823283T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823283T>A , CM000664.2:g.24823283T>A	GRCh38
NC_000002.11:g.25046152T>A , CM000664.1:g.25046152T>A	GRCh37
NC_000002.10:g.24899656T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2812A>T	ENSP00000384484.2:p.Thr938Ser
ENST00000679454.1:c.2809A>T MANE Select	ENSP00000505261.1:p.Thr937Ser
ENST00000260600.9:c.2809A>T	ENSP00000260600.5:p.Thr937Ser
ENST00000405392.5:c.2812A>T	ENSP00000384484.2:p.Thr938Ser
ENST00000485887.1:n.81A>T
ENST00000606682.5:c.1750A>T	ENSP00000475652.1:p.Thr584Ser
NM_004036.3:c.2809A>T	NP_004027.2:p.Thr937Ser
XM_005264104.1:c.2812A>T	XP_005264161.1:p.Thr938Ser
XM_005264105.1:c.2809A>T	XP_005264162.1:p.Thr937Ser
XM_006711925.1:c.2878A>T	XP_006711988.1:p.Thr960Ser
XM_011532489.1:c.2935A>T	XP_011530791.1:p.Thr979Ser
XM_011532490.1:c.2932A>T	XP_011530792.1:p.Thr978Ser
XM_011532491.1:c.2869A>T	XP_011530793.1:p.Thr957Ser
XM_011532492.1:c.2935A>T	XP_011530794.1:p.Thr979Ser
XM_011532493.1:c.2797A>T	XP_011530795.1:p.Thr933Ser
XM_011532494.1:c.2737A>T	XP_011530796.1:p.Thr913Ser
XM_011532495.1:c.2269A>T	XP_011530797.1:p.Thr757Ser
XM_011532496.1:c.2212A>T	XP_011530798.1:p.Thr738Ser
NM_001320613.1:c.2812A>T	NP_001307542.1:p.Thr938Ser
NM_004036.4:c.2809A>T	NP_004027.2:p.Thr937Ser
XM_011532492.2:c.2935A>T	XP_011530794.1:p.Thr979Ser
XM_017003186.1:c.2875A>T	XP_016858675.1:p.Thr959Ser
XM_017003187.1:c.2866A>T	XP_016858676.1:p.Thr956Ser
XM_017003188.1:c.2932A>T	XP_016858677.1:p.Thr978Ser
XM_017003189.1:c.2794A>T	XP_016858678.1:p.Thr932Ser
XM_017003190.1:c.2671A>T	XP_016858679.1:p.Thr891Ser
XM_017003191.1:c.2299A>T	XP_016858680.1:p.Thr767Ser
XM_017003192.1:c.2089A>T	XP_016858681.1:p.Thr697Ser
XM_017003193.1:c.2086A>T	XP_016858682.1:p.Thr696Ser
NM_001320613.2:c.2812A>T	NP_001307542.1:p.Thr938Ser
NM_001377128.1:c.2875A>T	NP_001364057.1:p.Thr959Ser
NM_001377129.1:c.2671A>T	NP_001364058.1:p.Thr891Ser
NM_001377130.1:c.2332-653A>T	NP_001364059.1:n.2332-653A>T
NM_001377131.1:c.2086A>T	NP_001364060.1:p.Thr696Ser
NM_001377132.1:c.2809A>T	NP_001364061.1:p.Thr937Ser
NM_004036.5:c.2809A>T MANE Select	NP_004027.2:p.Thr937Ser