Canonical Allele Identifier: CA1553681

Gene: ADCY3

Linked Data

• dbSNP Id: rs763507813
• ExAC: 2:25047454 TAGA / T
• gnomAD v2: 2-25047454-TAGA-T
• MyVariant Identifiers: chr2:g.25047455_25047457del (hg19) ; chr2:g.24824586_24824588del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824588_24824590del , CM000664.2:g.24824588_24824590del	GRCh38
NC_000002.11:g.25047457_25047459del , CM000664.1:g.25047457_25047459del	GRCh37
NC_000002.10:g.24900961_24900963del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2581-52_2581-50del	ENSP00000384484.2:n.2581-52_2581-50del
ENST00000679454.1:c.2578-52_2578-50del MANE Select	ENSP00000505261.1:n.2578-52_2578-50del
ENST00000260600.9:c.2578-52_2578-50del	ENSP00000260600.5:n.2578-52_2578-50del
ENST00000405392.5:c.2581-52_2581-50del	ENSP00000384484.2:n.2581-52_2581-50del
ENST00000606682.5:c.1519-52_1519-50del	ENSP00000475652.1:n.1519-52_1519-50del
NM_004036.3:c.2578-52_2578-50del	NP_004027.2:n.2578-52_2578-50del
XM_005264104.1:c.2581-52_2581-50del	XP_005264161.1:n.2581-52_2581-50del
XM_005264105.1:c.2578-52_2578-50del	XP_005264162.1:n.2578-52_2578-50del
XM_006711925.1:c.2647-52_2647-50del	XP_006711988.1:n.2647-52_2647-50del
XM_011532489.1:c.2704-52_2704-50del	XP_011530791.1:n.2704-52_2704-50del
XM_011532490.1:c.2701-52_2701-50del	XP_011530792.1:n.2701-52_2701-50del
XM_011532491.1:c.2638-52_2638-50del	XP_011530793.1:n.2638-52_2638-50del
XM_011532492.1:c.2704-52_2704-50del	XP_011530794.1:n.2704-52_2704-50del
XM_011532493.1:c.2566-52_2566-50del	XP_011530795.1:n.2566-52_2566-50del
XM_011532494.1:c.2506-52_2506-50del	XP_011530796.1:n.2506-52_2506-50del
XM_011532495.1:c.2038-52_2038-50del	XP_011530797.1:n.2038-52_2038-50del
XM_011532496.1:c.1981-52_1981-50del	XP_011530798.1:n.1981-52_1981-50del
NM_001320613.1:c.2581-52_2581-50del	NP_001307542.1:n.2581-52_2581-50del
NM_004036.4:c.2578-52_2578-50del	NP_004027.2:n.2578-52_2578-50del
XM_011532492.2:c.2704-52_2704-50del	XP_011530794.1:n.2704-52_2704-50del
XM_017003186.1:c.2644-52_2644-50del	XP_016858675.1:n.2644-52_2644-50del
XM_017003187.1:c.2635-52_2635-50del	XP_016858676.1:n.2635-52_2635-50del
XM_017003188.1:c.2701-52_2701-50del	XP_016858677.1:n.2701-52_2701-50del
XM_017003189.1:c.2563-52_2563-50del	XP_016858678.1:n.2563-52_2563-50del
XM_017003190.1:c.2440-52_2440-50del	XP_016858679.1:n.2440-52_2440-50del
XM_017003191.1:c.2068-52_2068-50del	XP_016858680.1:n.2068-52_2068-50del
XM_017003192.1:c.1858-52_1858-50del	XP_016858681.1:n.1858-52_1858-50del
XM_017003193.1:c.1855-52_1855-50del	XP_016858682.1:n.1855-52_1855-50del
NM_001320613.2:c.2581-52_2581-50del	NP_001307542.1:n.2581-52_2581-50del
NM_001377128.1:c.2644-52_2644-50del	NP_001364057.1:n.2644-52_2644-50del
NM_001377129.1:c.2440-52_2440-50del	NP_001364058.1:n.2440-52_2440-50del
NM_001377130.1:c.2173-52_2173-50del	NP_001364059.1:n.2173-52_2173-50del
NM_001377131.1:c.1855-52_1855-50del	NP_001364060.1:n.1855-52_1855-50del
NM_001377132.1:c.2578-52_2578-50del	NP_001364061.1:n.2578-52_2578-50del
NM_004036.5:c.2578-52_2578-50del MANE Select	NP_004027.2:n.2578-52_2578-50del