Canonical Allele Identifier: CA425171992

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046150T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823281T>G , CM000664.2:g.24823281T>G	GRCh38
NC_000002.11:g.25046150T>G , CM000664.1:g.25046150T>G	GRCh37
NC_000002.10:g.24899654T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2814A>C	ENSP00000384484.2:p.Thr938=
ENST00000679454.1:c.2811A>C MANE Select	ENSP00000505261.1:p.Thr937=
ENST00000260600.9:c.2811A>C	ENSP00000260600.5:p.Thr937=
ENST00000405392.5:c.2814A>C	ENSP00000384484.2:p.Thr938=
ENST00000485887.1:n.83A>C
ENST00000606682.5:c.1752A>C	ENSP00000475652.1:p.Thr584=
NM_004036.3:c.2811A>C	NP_004027.2:p.Thr937=
XM_005264104.1:c.2814A>C	XP_005264161.1:p.Thr938=
XM_005264105.1:c.2811A>C	XP_005264162.1:p.Thr937=
XM_006711925.1:c.2880A>C	XP_006711988.1:p.Thr960=
XM_011532489.1:c.2937A>C	XP_011530791.1:p.Thr979=
XM_011532490.1:c.2934A>C	XP_011530792.1:p.Thr978=
XM_011532491.1:c.2871A>C	XP_011530793.1:p.Thr957=
XM_011532492.1:c.2937A>C	XP_011530794.1:p.Thr979=
XM_011532493.1:c.2799A>C	XP_011530795.1:p.Thr933=
XM_011532494.1:c.2739A>C	XP_011530796.1:p.Thr913=
XM_011532495.1:c.2271A>C	XP_011530797.1:p.Thr757=
XM_011532496.1:c.2214A>C	XP_011530798.1:p.Thr738=
NM_001320613.1:c.2814A>C	NP_001307542.1:p.Thr938=
NM_004036.4:c.2811A>C	NP_004027.2:p.Thr937=
XM_011532492.2:c.2937A>C	XP_011530794.1:p.Thr979=
XM_017003186.1:c.2877A>C	XP_016858675.1:p.Thr959=
XM_017003187.1:c.2868A>C	XP_016858676.1:p.Thr956=
XM_017003188.1:c.2934A>C	XP_016858677.1:p.Thr978=
XM_017003189.1:c.2796A>C	XP_016858678.1:p.Thr932=
XM_017003190.1:c.2673A>C	XP_016858679.1:p.Thr891=
XM_017003191.1:c.2301A>C	XP_016858680.1:p.Thr767=
XM_017003192.1:c.2091A>C	XP_016858681.1:p.Thr697=
XM_017003193.1:c.2088A>C	XP_016858682.1:p.Thr696=
NM_001320613.2:c.2814A>C	NP_001307542.1:p.Thr938=
NM_001377128.1:c.2877A>C	NP_001364057.1:p.Thr959=
NM_001377129.1:c.2673A>C	NP_001364058.1:p.Thr891=
NM_001377130.1:c.2332-651A>C	NP_001364059.1:n.2332-651A>C
NM_001377131.1:c.2088A>C	NP_001364060.1:p.Thr696=
NM_001377132.1:c.2811A>C	NP_001364061.1:p.Thr937=
NM_004036.5:c.2811A>C MANE Select	NP_004027.2:p.Thr937=