Canonical Allele Identifier: CA2749194432

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24831216_24831230del , CM000664.2:g.24831216_24831230del	GRCh38
NC_000002.11:g.25054085_25054099del , CM000664.1:g.25054085_25054099del	GRCh37
NC_000002.10:g.24907589_24907603del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2056-405_2056-391del	ENSP00000384484.2:n.2056-405_2056-391del
ENST00000679454.1:c.2056-405_2056-391del MANE Select	ENSP00000505261.1:n.2056-405_2056-391del
ENST00000260600.9:c.2056-405_2056-391del	ENSP00000260600.5:n.2056-405_2056-391del
ENST00000405392.5:c.2056-405_2056-391del	ENSP00000384484.2:n.2056-405_2056-391del
ENST00000450524.1:n.149-405_149-391del
ENST00000455323.1:c.73-405_73-391del	ENSP00000402008.1:n.73-405_73-391del
ENST00000606682.5:c.1135-405_1135-391del	ENSP00000475652.1:n.1135-405_1135-391del
NM_004036.3:c.2056-405_2056-391del	NP_004027.2:n.2056-405_2056-391del
XM_005264104.1:c.2056-405_2056-391del	XP_005264161.1:n.2056-405_2056-391del
XM_005264105.1:c.2056-405_2056-391del	XP_005264162.1:n.2056-405_2056-391del
XM_006711925.1:c.2122-405_2122-391del	XP_006711988.1:n.2122-405_2122-391del
XM_011532489.1:c.2179-405_2179-391del	XP_011530791.1:n.2179-405_2179-391del
XM_011532490.1:c.2179-405_2179-391del	XP_011530792.1:n.2179-405_2179-391del
XM_011532491.1:c.2113-405_2113-391del	XP_011530793.1:n.2113-405_2113-391del
XM_011532492.1:c.2179-405_2179-391del	XP_011530794.1:n.2179-405_2179-391del
XM_011532493.1:c.2179-405_2179-391del	XP_011530795.1:n.2179-405_2179-391del
XM_011532494.1:c.2122-405_2122-391del	XP_011530796.1:n.2122-405_2122-391del
XM_011532495.1:c.1513-405_1513-391del	XP_011530797.1:n.1513-405_1513-391del
XM_011532496.1:c.1456-405_1456-391del	XP_011530798.1:n.1456-405_1456-391del
NM_001320613.1:c.2056-405_2056-391del	NP_001307542.1:n.2056-405_2056-391del
NM_004036.4:c.2056-405_2056-391del	NP_004027.2:n.2056-405_2056-391del
XM_011532492.2:c.2179-405_2179-391del	XP_011530794.1:n.2179-405_2179-391del
XM_017003186.1:c.2122-405_2122-391del	XP_016858675.1:n.2122-405_2122-391del
XM_017003187.1:c.2113-405_2113-391del	XP_016858676.1:n.2113-405_2113-391del
XM_017003188.1:c.2179-405_2179-391del	XP_016858677.1:n.2179-405_2179-391del
XM_017003189.1:c.2179-405_2179-391del	XP_016858678.1:n.2179-405_2179-391del
XM_017003190.1:c.2056-405_2056-391del	XP_016858679.1:n.2056-405_2056-391del
XM_017003191.1:c.1543-405_1543-391del	XP_016858680.1:n.1543-405_1543-391del
XM_017003192.1:c.1333-405_1333-391del	XP_016858681.1:n.1333-405_1333-391del
XM_017003193.1:c.1333-405_1333-391del	XP_016858682.1:n.1333-405_1333-391del
NM_001320613.2:c.2056-405_2056-391del	NP_001307542.1:n.2056-405_2056-391del
NM_001377128.1:c.2122-405_2122-391del	NP_001364057.1:n.2122-405_2122-391del
NM_001377129.1:c.2056-405_2056-391del	NP_001364058.1:n.2056-405_2056-391del
NM_001377130.1:c.2056-405_2056-391del	NP_001364059.1:n.2056-405_2056-391del
NM_001377131.1:c.1333-405_1333-391del	NP_001364060.1:n.1333-405_1333-391del
NM_001377132.1:c.2056-405_2056-391del	NP_001364061.1:n.2056-405_2056-391del
NM_004036.5:c.2056-405_2056-391del MANE Select	NP_004027.2:n.2056-405_2056-391del