Canonical Allele Identifier: CA767116686

Gene: ADCY3

Linked Data

• dbSNP Id: rs1464086876
• MyVariant Identifiers: chr2:g.25046209_25046211del (hg19) ; chr2:g.24823340_24823342del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823340_24823342del , CM000664.2:g.24823340_24823342del	GRCh38
NC_000002.11:g.25046209_25046211del , CM000664.1:g.25046209_25046211del	GRCh37
NC_000002.10:g.24899713_24899715del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2753_2755del	ENSP00000384484.2:p.Gln918_Thr919delinsPro
ENST00000679454.1:c.2750_2752del MANE Select	ENSP00000505261.1:p.Gln917_Thr918delinsPro
ENST00000260600.9:c.2750_2752del	ENSP00000260600.5:p.Gln917_Thr918delinsPro
ENST00000405392.5:c.2753_2755del	ENSP00000384484.2:p.Gln918_Thr919delinsPro
ENST00000485887.1:n.22_24del
ENST00000606682.5:c.1691_1693del	ENSP00000475652.1:p.Gln564_Thr565delinsPro
NM_004036.3:c.2750_2752del	NP_004027.2:p.Gln917_Thr918delinsPro
XM_005264104.1:c.2753_2755del	XP_005264161.1:p.Gln918_Thr919delinsPro
XM_005264105.1:c.2750_2752del	XP_005264162.1:p.Gln917_Thr918delinsPro
XM_006711925.1:c.2819_2821del	XP_006711988.1:p.Gln940_Thr941delinsPro
XM_011532489.1:c.2876_2878del	XP_011530791.1:p.Gln959_Thr960delinsPro
XM_011532490.1:c.2873_2875del	XP_011530792.1:p.Gln958_Thr959delinsPro
XM_011532491.1:c.2810_2812del	XP_011530793.1:p.Gln937_Thr938delinsPro
XM_011532492.1:c.2876_2878del	XP_011530794.1:p.Gln959_Thr960delinsPro
XM_011532493.1:c.2738_2740del	XP_011530795.1:p.Gln913_Thr914delinsPro
XM_011532494.1:c.2678_2680del	XP_011530796.1:p.Gln893_Thr894delinsPro
XM_011532495.1:c.2210_2212del	XP_011530797.1:p.Gln737_Thr738delinsPro
XM_011532496.1:c.2153_2155del	XP_011530798.1:p.Gln718_Thr719delinsPro
NM_001320613.1:c.2753_2755del	NP_001307542.1:p.Gln918_Thr919delinsPro
NM_004036.4:c.2750_2752del	NP_004027.2:p.Gln917_Thr918delinsPro
XM_011532492.2:c.2876_2878del	XP_011530794.1:p.Gln959_Thr960delinsPro
XM_017003186.1:c.2816_2818del	XP_016858675.1:p.Gln939_Thr940delinsPro
XM_017003187.1:c.2807_2809del	XP_016858676.1:p.Gln936_Thr937delinsPro
XM_017003188.1:c.2873_2875del	XP_016858677.1:p.Gln958_Thr959delinsPro
XM_017003189.1:c.2735_2737del	XP_016858678.1:p.Gln912_Thr913delinsPro
XM_017003190.1:c.2612_2614del	XP_016858679.1:p.Gln871_Thr872delinsPro
XM_017003191.1:c.2240_2242del	XP_016858680.1:p.Gln747_Thr748delinsPro
XM_017003192.1:c.2030_2032del	XP_016858681.1:p.Gln677_Thr678delinsPro
XM_017003193.1:c.2027_2029del	XP_016858682.1:p.Gln676_Thr677delinsPro
NM_001320613.2:c.2753_2755del	NP_001307542.1:p.Gln918_Thr919delinsPro
NM_001377128.1:c.2816_2818del	NP_001364057.1:p.Gln939_Thr940delinsPro
NM_001377129.1:c.2612_2614del	NP_001364058.1:p.Gln871_Thr872delinsPro
NM_001377130.1:c.2332-712_2332-710del	NP_001364059.1:n.2332-712_2332-710del
NM_001377131.1:c.2027_2029del	NP_001364060.1:p.Gln676_Thr677delinsPro
NM_001377132.1:c.2750_2752del	NP_001364061.1:p.Gln917_Thr918delinsPro
NM_004036.5:c.2750_2752del MANE Select	NP_004027.2:p.Gln917_Thr918delinsPro