Canonical Allele Identifier: CA767114639

Gene: ADCY3

Linked Data

• dbSNP Id: rs10683974
• MyVariant Identifiers: chr2:g.25054113_25054114insAAC (hg19) ; chr2:g.24831244_24831245insAAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24831244_24831245insAAC , CM000664.2:g.24831244_24831245insAAC	GRCh38
NC_000002.11:g.25054113_25054114insAAC , CM000664.1:g.25054113_25054114insAAC	GRCh37
NC_000002.10:g.24907617_24907618insAAC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2055+417_2056-419insGTT	ENSP00000384484.2:n.2055+417_2056-419insGTT
ENST00000679454.1:c.2055+417_2056-419insGTT MANE Select	ENSP00000505261.1:n.2055+417_2056-419insGTT
ENST00000260600.9:c.2055+417_2056-419insGTT	ENSP00000260600.5:n.2055+417_2056-419insGTT
ENST00000405392.5:c.2055+417_2056-419insGTT	ENSP00000384484.2:n.2055+417_2056-419insGTT
ENST00000450524.1:n.148+417_149-419insGTT
ENST00000455323.1:c.72+417_73-419insGTT	ENSP00000402008.1:n.72+417_73-419insGTT
ENST00000606682.5:c.1134+417_1135-419insGTT	ENSP00000475652.1:n.1134+417_1135-419insGTT
NM_004036.3:c.2055+417_2056-419insGTT	NP_004027.2:n.2055+417_2056-419insGTT
XM_005264104.1:c.2055+417_2056-419insGTT	XP_005264161.1:n.2055+417_2056-419insGTT
XM_005264105.1:c.2055+417_2056-419insGTT	XP_005264162.1:n.2055+417_2056-419insGTT
XM_006711925.1:c.2121+417_2122-419insGTT	XP_006711988.1:n.2121+417_2122-419insGTT
XM_011532489.1:c.2178+417_2179-419insGTT	XP_011530791.1:n.2178+417_2179-419insGTT
XM_011532490.1:c.2178+417_2179-419insGTT	XP_011530792.1:n.2178+417_2179-419insGTT
XM_011532491.1:c.2112+417_2113-419insGTT	XP_011530793.1:n.2112+417_2113-419insGTT
XM_011532492.1:c.2178+417_2179-419insGTT	XP_011530794.1:n.2178+417_2179-419insGTT
XM_011532493.1:c.2178+417_2179-419insGTT	XP_011530795.1:n.2178+417_2179-419insGTT
XM_011532494.1:c.2121+417_2122-419insGTT	XP_011530796.1:n.2121+417_2122-419insGTT
XM_011532495.1:c.1512+417_1513-419insGTT	XP_011530797.1:n.1512+417_1513-419insGTT
XM_011532496.1:c.1455+417_1456-419insGTT	XP_011530798.1:n.1455+417_1456-419insGTT
NM_001320613.1:c.2055+417_2056-419insGTT	NP_001307542.1:n.2055+417_2056-419insGTT
NM_004036.4:c.2055+417_2056-419insGTT	NP_004027.2:n.2055+417_2056-419insGTT
XM_011532492.2:c.2178+417_2179-419insGTT	XP_011530794.1:n.2178+417_2179-419insGTT
XM_017003186.1:c.2121+417_2122-419insGTT	XP_016858675.1:n.2121+417_2122-419insGTT
XM_017003187.1:c.2112+417_2113-419insGTT	XP_016858676.1:n.2112+417_2113-419insGTT
XM_017003188.1:c.2178+417_2179-419insGTT	XP_016858677.1:n.2178+417_2179-419insGTT
XM_017003189.1:c.2178+417_2179-419insGTT	XP_016858678.1:n.2178+417_2179-419insGTT
XM_017003190.1:c.2055+417_2056-419insGTT	XP_016858679.1:n.2055+417_2056-419insGTT
XM_017003191.1:c.1542+417_1543-419insGTT	XP_016858680.1:n.1542+417_1543-419insGTT
XM_017003192.1:c.1332+417_1333-419insGTT	XP_016858681.1:n.1332+417_1333-419insGTT
XM_017003193.1:c.1332+417_1333-419insGTT	XP_016858682.1:n.1332+417_1333-419insGTT
NM_001320613.2:c.2055+417_2056-419insGTT	NP_001307542.1:n.2055+417_2056-419insGTT
NM_001377128.1:c.2121+417_2122-419insGTT	NP_001364057.1:n.2121+417_2122-419insGTT
NM_001377129.1:c.2055+417_2056-419insGTT	NP_001364058.1:n.2055+417_2056-419insGTT
NM_001377130.1:c.2055+417_2056-419insGTT	NP_001364059.1:n.2055+417_2056-419insGTT
NM_001377131.1:c.1332+417_1333-419insGTT	NP_001364060.1:n.1332+417_1333-419insGTT
NM_001377132.1:c.2055+417_2056-419insGTT	NP_001364061.1:n.2055+417_2056-419insGTT
NM_004036.5:c.2055+417_2056-419insGTT MANE Select	NP_004027.2:n.2055+417_2056-419insGTT