Canonical Allele Identifier: CA1239072928

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824456_24824457delinsGC , CM000664.2:g.24824456_24824457delinsGC	GRCh38
NC_000002.11:g.25047325_25047326delinsGC , CM000664.1:g.25047325_25047326delinsGC	GRCh37
NC_000002.10:g.24900829_24900830delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2660_2661delinsGC	ENSP00000384484.2:p.Arg887=
ENST00000679454.1:c.2657_2658delinsGC MANE Select	ENSP00000505261.1:p.Arg886=
ENST00000260600.9:c.2657_2658delinsGC	ENSP00000260600.5:p.Arg886=
ENST00000405392.5:c.2660_2661delinsGC	ENSP00000384484.2:p.Arg887=
ENST00000606682.5:c.1598_1599delinsGC	ENSP00000475652.1:p.Arg533=
NM_004036.3:c.2657_2658delinsGC	NP_004027.2:p.Arg886=
XM_005264104.1:c.2660_2661delinsGC	XP_005264161.1:p.Arg887=
XM_005264105.1:c.2657_2658delinsGC	XP_005264162.1:p.Arg886=
XM_006711925.1:c.2726_2727delinsGC	XP_006711988.1:p.Arg909=
XM_011532489.1:c.2783_2784delinsGC	XP_011530791.1:p.Arg928=
XM_011532490.1:c.2780_2781delinsGC	XP_011530792.1:p.Arg927=
XM_011532491.1:c.2717_2718delinsGC	XP_011530793.1:p.Arg906=
XM_011532492.1:c.2783_2784delinsGC	XP_011530794.1:p.Arg928=
XM_011532493.1:c.2645_2646delinsGC	XP_011530795.1:p.Arg882=
XM_011532494.1:c.2585_2586delinsGC	XP_011530796.1:p.Arg862=
XM_011532495.1:c.2117_2118delinsGC	XP_011530797.1:p.Arg706=
XM_011532496.1:c.2060_2061delinsGC	XP_011530798.1:p.Arg687=
NM_001320613.1:c.2660_2661delinsGC	NP_001307542.1:p.Arg887=
NM_004036.4:c.2657_2658delinsGC	NP_004027.2:p.Arg886=
XM_011532492.2:c.2783_2784delinsGC	XP_011530794.1:p.Arg928=
XM_017003186.1:c.2723_2724delinsGC	XP_016858675.1:p.Arg908=
XM_017003187.1:c.2714_2715delinsGC	XP_016858676.1:p.Arg905=
XM_017003188.1:c.2780_2781delinsGC	XP_016858677.1:p.Arg927=
XM_017003189.1:c.2642_2643delinsGC	XP_016858678.1:p.Arg881=
XM_017003190.1:c.2519_2520delinsGC	XP_016858679.1:p.Arg840=
XM_017003191.1:c.2147_2148delinsGC	XP_016858680.1:p.Arg716=
XM_017003192.1:c.1937_1938delinsGC	XP_016858681.1:p.Arg646=
XM_017003193.1:c.1934_1935delinsGC	XP_016858682.1:p.Arg645=
NM_001320613.2:c.2660_2661delinsGC	NP_001307542.1:p.Arg887=
NM_001377128.1:c.2723_2724delinsGC	NP_001364057.1:p.Arg908=
NM_001377129.1:c.2519_2520delinsGC	NP_001364058.1:p.Arg840=
NM_001377130.1:c.2252_2253delinsGC	NP_001364059.1:p.Arg751=
NM_001377131.1:c.1934_1935delinsGC	NP_001364060.1:p.Arg645=
NM_001377132.1:c.2657_2658delinsGC	NP_001364061.1:p.Arg886=
NM_004036.5:c.2657_2658delinsGC MANE Select	NP_004027.2:p.Arg886=