Canonical Allele Identifier: CA1239073055

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824686_24824687delinsCG , CM000664.2:g.24824686_24824687delinsCG	GRCh38
NC_000002.11:g.25047555_25047556delinsCG , CM000664.1:g.25047555_25047556delinsCG	GRCh37
NC_000002.10:g.24901059_24901060delinsCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2581-151_2581-150delinsCG	ENSP00000384484.2:n.2581-151_2581-150delinsCG
ENST00000679454.1:c.2578-151_2578-150delinsCG MANE Select	ENSP00000505261.1:n.2578-151_2578-150delinsCG
ENST00000260600.9:c.2578-151_2578-150delinsCG	ENSP00000260600.5:n.2578-151_2578-150delinsCG
ENST00000405392.5:c.2581-151_2581-150delinsCG	ENSP00000384484.2:n.2581-151_2581-150delinsCG
ENST00000606682.5:c.1519-151_1519-150delinsCG	ENSP00000475652.1:n.1519-151_1519-150delinsCG
NM_004036.3:c.2578-151_2578-150delinsCG	NP_004027.2:n.2578-151_2578-150delinsCG
XM_005264104.1:c.2581-151_2581-150delinsCG	XP_005264161.1:n.2581-151_2581-150delinsCG
XM_005264105.1:c.2578-151_2578-150delinsCG	XP_005264162.1:n.2578-151_2578-150delinsCG
XM_006711925.1:c.2647-151_2647-150delinsCG	XP_006711988.1:n.2647-151_2647-150delinsCG
XM_011532489.1:c.2704-151_2704-150delinsCG	XP_011530791.1:n.2704-151_2704-150delinsCG
XM_011532490.1:c.2701-151_2701-150delinsCG	XP_011530792.1:n.2701-151_2701-150delinsCG
XM_011532491.1:c.2638-151_2638-150delinsCG	XP_011530793.1:n.2638-151_2638-150delinsCG
XM_011532492.1:c.2704-151_2704-150delinsCG	XP_011530794.1:n.2704-151_2704-150delinsCG
XM_011532493.1:c.2566-151_2566-150delinsCG	XP_011530795.1:n.2566-151_2566-150delinsCG
XM_011532494.1:c.2506-151_2506-150delinsCG	XP_011530796.1:n.2506-151_2506-150delinsCG
XM_011532495.1:c.2038-151_2038-150delinsCG	XP_011530797.1:n.2038-151_2038-150delinsCG
XM_011532496.1:c.1981-151_1981-150delinsCG	XP_011530798.1:n.1981-151_1981-150delinsCG
NM_001320613.1:c.2581-151_2581-150delinsCG	NP_001307542.1:n.2581-151_2581-150delinsCG
NM_004036.4:c.2578-151_2578-150delinsCG	NP_004027.2:n.2578-151_2578-150delinsCG
XM_011532492.2:c.2704-151_2704-150delinsCG	XP_011530794.1:n.2704-151_2704-150delinsCG
XM_017003186.1:c.2644-151_2644-150delinsCG	XP_016858675.1:n.2644-151_2644-150delinsCG
XM_017003187.1:c.2635-151_2635-150delinsCG	XP_016858676.1:n.2635-151_2635-150delinsCG
XM_017003188.1:c.2701-151_2701-150delinsCG	XP_016858677.1:n.2701-151_2701-150delinsCG
XM_017003189.1:c.2563-151_2563-150delinsCG	XP_016858678.1:n.2563-151_2563-150delinsCG
XM_017003190.1:c.2440-151_2440-150delinsCG	XP_016858679.1:n.2440-151_2440-150delinsCG
XM_017003191.1:c.2068-151_2068-150delinsCG	XP_016858680.1:n.2068-151_2068-150delinsCG
XM_017003192.1:c.1858-151_1858-150delinsCG	XP_016858681.1:n.1858-151_1858-150delinsCG
XM_017003193.1:c.1855-151_1855-150delinsCG	XP_016858682.1:n.1855-151_1855-150delinsCG
NM_001320613.2:c.2581-151_2581-150delinsCG	NP_001307542.1:n.2581-151_2581-150delinsCG
NM_001377128.1:c.2644-151_2644-150delinsCG	NP_001364057.1:n.2644-151_2644-150delinsCG
NM_001377129.1:c.2440-151_2440-150delinsCG	NP_001364058.1:n.2440-151_2440-150delinsCG
NM_001377130.1:c.2173-151_2173-150delinsCG	NP_001364059.1:n.2173-151_2173-150delinsCG
NM_001377131.1:c.1855-151_1855-150delinsCG	NP_001364060.1:n.1855-151_1855-150delinsCG
NM_001377132.1:c.2578-151_2578-150delinsCG	NP_001364061.1:n.2578-151_2578-150delinsCG
NM_004036.5:c.2578-151_2578-150delinsCG MANE Select	NP_004027.2:n.2578-151_2578-150delinsCG