Canonical Allele Identifier: CA2658139569

Gene: ADCY3

Linked Data

• gnomAD v4: 2-24823233-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823235del , CM000664.2:g.24823235del	GRCh38
NC_000002.11:g.25046104del , CM000664.1:g.25046104del	GRCh37
NC_000002.10:g.24899608del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2861del	ENSP00000384484.2:p.Asn954MetfsTer18
ENST00000679454.1:c.2858del MANE Select	ENSP00000505261.1:p.Asn953MetfsTer18
ENST00000260600.9:c.2858del	ENSP00000260600.5:p.Asn953MetfsTer18
ENST00000405392.5:c.2861del	ENSP00000384484.2:p.Asn954MetfsTer18
ENST00000485887.1:n.130del
ENST00000606682.5:c.1799del	ENSP00000475652.1:p.Asn600MetfsTer18
NM_004036.3:c.2858del	NP_004027.2:p.Asn953MetfsTer18
XM_005264104.1:c.2861del	XP_005264161.1:p.Asn954MetfsTer18
XM_005264105.1:c.2858del	XP_005264162.1:p.Asn953MetfsTer18
XM_006711925.1:c.2927del	XP_006711988.1:p.Asn976MetfsTer18
XM_011532489.1:c.2984del	XP_011530791.1:p.Asn995MetfsTer18
XM_011532490.1:c.2981del	XP_011530792.1:p.Asn994MetfsTer18
XM_011532491.1:c.2918del	XP_011530793.1:p.Asn973MetfsTer18
XM_011532492.1:c.2984del	XP_011530794.1:p.Asn995MetfsTer18
XM_011532493.1:c.2846del	XP_011530795.1:p.Asn949MetfsTer18
XM_011532494.1:c.2786del	XP_011530796.1:p.Asn929MetfsTer18
XM_011532495.1:c.2318del	XP_011530797.1:p.Asn773MetfsTer18
XM_011532496.1:c.2261del	XP_011530798.1:p.Asn754MetfsTer18
NM_001320613.1:c.2861del	NP_001307542.1:p.Asn954MetfsTer18
NM_004036.4:c.2858del	NP_004027.2:p.Asn953MetfsTer18
XM_011532492.2:c.2984del	XP_011530794.1:p.Asn995MetfsTer18
XM_017003186.1:c.2924del	XP_016858675.1:p.Asn975MetfsTer18
XM_017003187.1:c.2915del	XP_016858676.1:p.Asn972MetfsTer18
XM_017003188.1:c.2981del	XP_016858677.1:p.Asn994MetfsTer18
XM_017003189.1:c.2843del	XP_016858678.1:p.Asn948MetfsTer18
XM_017003190.1:c.2720del	XP_016858679.1:p.Asn907MetfsTer18
XM_017003191.1:c.2348del	XP_016858680.1:p.Asn783MetfsTer18
XM_017003192.1:c.2138del	XP_016858681.1:p.Asn713MetfsTer18
XM_017003193.1:c.2135del	XP_016858682.1:p.Asn712MetfsTer18
NM_001320613.2:c.2861del	NP_001307542.1:p.Asn954MetfsTer18
NM_001377128.1:c.2924del	NP_001364057.1:p.Asn975MetfsTer18
NM_001377129.1:c.2720del	NP_001364058.1:p.Asn907MetfsTer18
NM_001377130.1:c.2332-604del	NP_001364059.1:n.2332-604del
NM_001377131.1:c.2135del	NP_001364060.1:p.Asn712MetfsTer18
NM_001377132.1:c.2858del	NP_001364061.1:p.Asn953MetfsTer18
NM_004036.5:c.2858del MANE Select	NP_004027.2:p.Asn953MetfsTer18