Canonical Allele Identifier: CA2749194433

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24831223_24831226del , CM000664.2:g.24831223_24831226del	GRCh38
NC_000002.11:g.25054092_25054095del , CM000664.1:g.25054092_25054095del	GRCh37
NC_000002.10:g.24907596_24907599del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2056-401_2056-398del	ENSP00000384484.2:n.2056-401_2056-398del
ENST00000679454.1:c.2056-401_2056-398del MANE Select	ENSP00000505261.1:n.2056-401_2056-398del
ENST00000260600.9:c.2056-401_2056-398del	ENSP00000260600.5:n.2056-401_2056-398del
ENST00000405392.5:c.2056-401_2056-398del	ENSP00000384484.2:n.2056-401_2056-398del
ENST00000450524.1:n.149-401_149-398del
ENST00000455323.1:c.73-401_73-398del	ENSP00000402008.1:n.73-401_73-398del
ENST00000606682.5:c.1135-401_1135-398del	ENSP00000475652.1:n.1135-401_1135-398del
NM_004036.3:c.2056-401_2056-398del	NP_004027.2:n.2056-401_2056-398del
XM_005264104.1:c.2056-401_2056-398del	XP_005264161.1:n.2056-401_2056-398del
XM_005264105.1:c.2056-401_2056-398del	XP_005264162.1:n.2056-401_2056-398del
XM_006711925.1:c.2122-401_2122-398del	XP_006711988.1:n.2122-401_2122-398del
XM_011532489.1:c.2179-401_2179-398del	XP_011530791.1:n.2179-401_2179-398del
XM_011532490.1:c.2179-401_2179-398del	XP_011530792.1:n.2179-401_2179-398del
XM_011532491.1:c.2113-401_2113-398del	XP_011530793.1:n.2113-401_2113-398del
XM_011532492.1:c.2179-401_2179-398del	XP_011530794.1:n.2179-401_2179-398del
XM_011532493.1:c.2179-401_2179-398del	XP_011530795.1:n.2179-401_2179-398del
XM_011532494.1:c.2122-401_2122-398del	XP_011530796.1:n.2122-401_2122-398del
XM_011532495.1:c.1513-401_1513-398del	XP_011530797.1:n.1513-401_1513-398del
XM_011532496.1:c.1456-401_1456-398del	XP_011530798.1:n.1456-401_1456-398del
NM_001320613.1:c.2056-401_2056-398del	NP_001307542.1:n.2056-401_2056-398del
NM_004036.4:c.2056-401_2056-398del	NP_004027.2:n.2056-401_2056-398del
XM_011532492.2:c.2179-401_2179-398del	XP_011530794.1:n.2179-401_2179-398del
XM_017003186.1:c.2122-401_2122-398del	XP_016858675.1:n.2122-401_2122-398del
XM_017003187.1:c.2113-401_2113-398del	XP_016858676.1:n.2113-401_2113-398del
XM_017003188.1:c.2179-401_2179-398del	XP_016858677.1:n.2179-401_2179-398del
XM_017003189.1:c.2179-401_2179-398del	XP_016858678.1:n.2179-401_2179-398del
XM_017003190.1:c.2056-401_2056-398del	XP_016858679.1:n.2056-401_2056-398del
XM_017003191.1:c.1543-401_1543-398del	XP_016858680.1:n.1543-401_1543-398del
XM_017003192.1:c.1333-401_1333-398del	XP_016858681.1:n.1333-401_1333-398del
XM_017003193.1:c.1333-401_1333-398del	XP_016858682.1:n.1333-401_1333-398del
NM_001320613.2:c.2056-401_2056-398del	NP_001307542.1:n.2056-401_2056-398del
NM_001377128.1:c.2122-401_2122-398del	NP_001364057.1:n.2122-401_2122-398del
NM_001377129.1:c.2056-401_2056-398del	NP_001364058.1:n.2056-401_2056-398del
NM_001377130.1:c.2056-401_2056-398del	NP_001364059.1:n.2056-401_2056-398del
NM_001377131.1:c.1333-401_1333-398del	NP_001364060.1:n.1333-401_1333-398del
NM_001377132.1:c.2056-401_2056-398del	NP_001364061.1:n.2056-401_2056-398del
NM_004036.5:c.2056-401_2056-398del MANE Select	NP_004027.2:n.2056-401_2056-398del