Canonical Allele Identifier: CA1028473432

Gene: ADCY3

Linked Data

• dbSNP Id: rs1668060670
• gnomAD v3: 2-24823329-CTCA-C
• gnomAD v4: 2-24823329-CTCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823334_24823336del , CM000664.2:g.24823334_24823336del	GRCh38
NC_000002.11:g.25046203_25046205del , CM000664.1:g.25046203_25046205del	GRCh37
NC_000002.10:g.24899707_24899709del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2763_2765del	ENSP00000384484.2:p.Asp921del
ENST00000679454.1:c.2760_2762del MANE Select	ENSP00000505261.1:p.Asp920del
ENST00000260600.9:c.2760_2762del	ENSP00000260600.5:p.Asp920del
ENST00000405392.5:c.2763_2765del	ENSP00000384484.2:p.Asp921del
ENST00000485887.1:n.32_34del
ENST00000606682.5:c.1701_1703del	ENSP00000475652.1:p.Asp567del
NM_004036.3:c.2760_2762del	NP_004027.2:p.Asp920del
XM_005264104.1:c.2763_2765del	XP_005264161.1:p.Asp921del
XM_005264105.1:c.2760_2762del	XP_005264162.1:p.Asp920del
XM_006711925.1:c.2829_2831del	XP_006711988.1:p.Asp943del
XM_011532489.1:c.2886_2888del	XP_011530791.1:p.Asp962del
XM_011532490.1:c.2883_2885del	XP_011530792.1:p.Asp961del
XM_011532491.1:c.2820_2822del	XP_011530793.1:p.Asp940del
XM_011532492.1:c.2886_2888del	XP_011530794.1:p.Asp962del
XM_011532493.1:c.2748_2750del	XP_011530795.1:p.Asp916del
XM_011532494.1:c.2688_2690del	XP_011530796.1:p.Asp896del
XM_011532495.1:c.2220_2222del	XP_011530797.1:p.Asp740del
XM_011532496.1:c.2163_2165del	XP_011530798.1:p.Asp721del
NM_001320613.1:c.2763_2765del	NP_001307542.1:p.Asp921del
NM_004036.4:c.2760_2762del	NP_004027.2:p.Asp920del
XM_011532492.2:c.2886_2888del	XP_011530794.1:p.Asp962del
XM_017003186.1:c.2826_2828del	XP_016858675.1:p.Asp942del
XM_017003187.1:c.2817_2819del	XP_016858676.1:p.Asp939del
XM_017003188.1:c.2883_2885del	XP_016858677.1:p.Asp961del
XM_017003189.1:c.2745_2747del	XP_016858678.1:p.Asp915del
XM_017003190.1:c.2622_2624del	XP_016858679.1:p.Asp874del
XM_017003191.1:c.2250_2252del	XP_016858680.1:p.Asp750del
XM_017003192.1:c.2040_2042del	XP_016858681.1:p.Asp680del
XM_017003193.1:c.2037_2039del	XP_016858682.1:p.Asp679del
NM_001320613.2:c.2763_2765del	NP_001307542.1:p.Asp921del
NM_001377128.1:c.2826_2828del	NP_001364057.1:p.Asp942del
NM_001377129.1:c.2622_2624del	NP_001364058.1:p.Asp874del
NM_001377130.1:c.2332-702_2332-700del	NP_001364059.1:n.2332-702_2332-700del
NM_001377131.1:c.2037_2039del	NP_001364060.1:p.Asp679del
NM_001377132.1:c.2760_2762del	NP_001364061.1:p.Asp920del
NM_004036.5:c.2760_2762del MANE Select	NP_004027.2:p.Asp920del