Canonical Allele Identifier: CA1028487759
Gene: ADCY3 HGNC NCBI

Linked Data

dbSNP Id: rs1669451787

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24831230_24831231insTA , CM000664.2:g.24831230_24831231insTA GRCh38
NC_000002.11:g.25054099_25054100insTA , CM000664.1:g.25054099_25054100insTA GRCh37
NC_000002.10:g.24907603_24907604insTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2056-406_2056-405insTA ENSP00000384484.2:n.2056-406_2056-405insTA
ENST00000679454.1:c.2056-406_2056-405insTA MANE Select ENSP00000505261.1:n.2056-406_2056-405insTA
ENST00000260600.9:c.2056-406_2056-405insTA ENSP00000260600.5:n.2056-406_2056-405insTA
ENST00000405392.5:c.2056-406_2056-405insTA ENSP00000384484.2:n.2056-406_2056-405insTA
ENST00000450524.1:n.149-406_149-405insTA
ENST00000455323.1:c.73-406_73-405insTA ENSP00000402008.1:n.73-406_73-405insTA
ENST00000606682.5:c.1135-406_1135-405insTA ENSP00000475652.1:n.1135-406_1135-405insTA
NM_004036.3:c.2056-406_2056-405insTA NP_004027.2:n.2056-406_2056-405insTA
XM_005264104.1:c.2056-406_2056-405insTA XP_005264161.1:n.2056-406_2056-405insTA
XM_005264105.1:c.2056-406_2056-405insTA XP_005264162.1:n.2056-406_2056-405insTA
XM_006711925.1:c.2122-406_2122-405insTA XP_006711988.1:n.2122-406_2122-405insTA
XM_011532489.1:c.2179-406_2179-405insTA XP_011530791.1:n.2179-406_2179-405insTA
XM_011532490.1:c.2179-406_2179-405insTA XP_011530792.1:n.2179-406_2179-405insTA
XM_011532491.1:c.2113-406_2113-405insTA XP_011530793.1:n.2113-406_2113-405insTA
XM_011532492.1:c.2179-406_2179-405insTA XP_011530794.1:n.2179-406_2179-405insTA
XM_011532493.1:c.2179-406_2179-405insTA XP_011530795.1:n.2179-406_2179-405insTA
XM_011532494.1:c.2122-406_2122-405insTA XP_011530796.1:n.2122-406_2122-405insTA
XM_011532495.1:c.1513-406_1513-405insTA XP_011530797.1:n.1513-406_1513-405insTA
XM_011532496.1:c.1456-406_1456-405insTA XP_011530798.1:n.1456-406_1456-405insTA
NM_001320613.1:c.2056-406_2056-405insTA NP_001307542.1:n.2056-406_2056-405insTA
NM_004036.4:c.2056-406_2056-405insTA NP_004027.2:n.2056-406_2056-405insTA
XM_011532492.2:c.2179-406_2179-405insTA XP_011530794.1:n.2179-406_2179-405insTA
XM_017003186.1:c.2122-406_2122-405insTA XP_016858675.1:n.2122-406_2122-405insTA
XM_017003187.1:c.2113-406_2113-405insTA XP_016858676.1:n.2113-406_2113-405insTA
XM_017003188.1:c.2179-406_2179-405insTA XP_016858677.1:n.2179-406_2179-405insTA
XM_017003189.1:c.2179-406_2179-405insTA XP_016858678.1:n.2179-406_2179-405insTA
XM_017003190.1:c.2056-406_2056-405insTA XP_016858679.1:n.2056-406_2056-405insTA
XM_017003191.1:c.1543-406_1543-405insTA XP_016858680.1:n.1543-406_1543-405insTA
XM_017003192.1:c.1333-406_1333-405insTA XP_016858681.1:n.1333-406_1333-405insTA
XM_017003193.1:c.1333-406_1333-405insTA XP_016858682.1:n.1333-406_1333-405insTA
NM_001320613.2:c.2056-406_2056-405insTA NP_001307542.1:n.2056-406_2056-405insTA
NM_001377128.1:c.2122-406_2122-405insTA NP_001364057.1:n.2122-406_2122-405insTA
NM_001377129.1:c.2056-406_2056-405insTA NP_001364058.1:n.2056-406_2056-405insTA
NM_001377130.1:c.2056-406_2056-405insTA NP_001364059.1:n.2056-406_2056-405insTA
NM_001377131.1:c.1333-406_1333-405insTA NP_001364060.1:n.1333-406_1333-405insTA
NM_001377132.1:c.2056-406_2056-405insTA NP_001364061.1:n.2056-406_2056-405insTA
NM_004036.5:c.2056-406_2056-405insTA MANE Select NP_004027.2:n.2056-406_2056-405insTA