Canonical Allele Identifier: CA2658143304

Gene: ADCY3

Linked Data

• gnomAD v4: 2-24841242-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24841242A>G , CM000664.2:g.24841242A>G	GRCh38
NC_000002.11:g.25064111A>G , CM000664.1:g.25064111A>G	GRCh37
NC_000002.10:g.24917615A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.1196+17T>C	ENSP00000384484.2:n.1196+17T>C
ENST00000679454.1:c.1196+17T>C MANE Select	ENSP00000505261.1:n.1196+17T>C
ENST00000260600.9:c.1196+17T>C	ENSP00000260600.5:n.1196+17T>C
ENST00000405392.5:c.1196+17T>C	ENSP00000384484.2:n.1196+17T>C
ENST00000427849.5:c.464+17T>C	ENSP00000399275.1:n.464+17T>C
ENST00000435135.5:c.1046+17T>C	ENSP00000389799.1:n.1046+17T>C
ENST00000479517.1:n.579+17T>C
ENST00000606682.5:c.209+17T>C	ENSP00000475652.1:n.209+17T>C
NM_004036.3:c.1196+17T>C	NP_004027.2:n.1196+17T>C
XM_005264104.1:c.1196+17T>C	XP_005264161.1:n.1196+17T>C
XM_005264105.1:c.1196+17T>C	XP_005264162.1:n.1196+17T>C
XM_006711925.1:c.1196+17T>C	XP_006711988.1:n.1196+17T>C
XM_011532489.1:c.1196+17T>C	XP_011530791.1:n.1196+17T>C
XM_011532490.1:c.1196+17T>C	XP_011530792.1:n.1196+17T>C
XM_011532491.1:c.1196+17T>C	XP_011530793.1:n.1196+17T>C
XM_011532492.1:c.1196+17T>C	XP_011530794.1:n.1196+17T>C
XM_011532493.1:c.1196+17T>C	XP_011530795.1:n.1196+17T>C
XM_011532494.1:c.1196+17T>C	XP_011530796.1:n.1196+17T>C
XM_011532495.1:c.530+17T>C	XP_011530797.1:n.530+17T>C
XM_011532496.1:c.473+17T>C	XP_011530798.1:n.473+17T>C
NM_001320613.1:c.1196+17T>C	NP_001307542.1:n.1196+17T>C
NM_004036.4:c.1196+17T>C	NP_004027.2:n.1196+17T>C
XM_011532492.2:c.1196+17T>C	XP_011530794.1:n.1196+17T>C
XM_017003186.1:c.1196+17T>C	XP_016858675.1:n.1196+17T>C
XM_017003187.1:c.1196+17T>C	XP_016858676.1:n.1196+17T>C
XM_017003188.1:c.1196+17T>C	XP_016858677.1:n.1196+17T>C
XM_017003189.1:c.1196+17T>C	XP_016858678.1:n.1196+17T>C
XM_017003190.1:c.1196+17T>C	XP_016858679.1:n.1196+17T>C
XM_017003191.1:c.560+17T>C	XP_016858680.1:n.560+17T>C
XM_017003192.1:c.473+17T>C	XP_016858681.1:n.473+17T>C
XM_017003193.1:c.473+17T>C	XP_016858682.1:n.473+17T>C
NM_001320613.2:c.1196+17T>C	NP_001307542.1:n.1196+17T>C
NM_001377128.1:c.1196+17T>C	NP_001364057.1:n.1196+17T>C
NM_001377129.1:c.1196+17T>C	NP_001364058.1:n.1196+17T>C
NM_001377130.1:c.1196+17T>C	NP_001364059.1:n.1196+17T>C
NM_001377131.1:c.473+17T>C	NP_001364060.1:n.473+17T>C
NM_001377132.1:c.1196+17T>C	NP_001364061.1:n.1196+17T>C
NM_004036.5:c.1196+17T>C MANE Select	NP_004027.2:n.1196+17T>C