Canonical Allele Identifier: CA346063659

Gene: ADCY3

Linked Data

• dbSNP Id: rs1157915112
• COSMIC: COSM4093238
• MyVariant Identifiers: chr2:g.25047330G>A (hg19) ; chr2:g.24824461G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824461G>A , CM000664.2:g.24824461G>A	GRCh38
NC_000002.11:g.25047330G>A , CM000664.1:g.25047330G>A	GRCh37
NC_000002.10:g.24900834G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2656C>T	ENSP00000384484.2:p.Arg886Ter
ENST00000679454.1:c.2653C>T MANE Select	ENSP00000505261.1:p.Arg885Ter
ENST00000260600.9:c.2653C>T	ENSP00000260600.5:p.Arg885Ter
ENST00000405392.5:c.2656C>T	ENSP00000384484.2:p.Arg886Ter
ENST00000606682.5:c.1594C>T	ENSP00000475652.1:p.Arg532Ter
NM_004036.3:c.2653C>T	NP_004027.2:p.Arg885Ter
XM_005264104.1:c.2656C>T	XP_005264161.1:p.Arg886Ter
XM_005264105.1:c.2653C>T	XP_005264162.1:p.Arg885Ter
XM_006711925.1:c.2722C>T	XP_006711988.1:p.Arg908Ter
XM_011532489.1:c.2779C>T	XP_011530791.1:p.Arg927Ter
XM_011532490.1:c.2776C>T	XP_011530792.1:p.Arg926Ter
XM_011532491.1:c.2713C>T	XP_011530793.1:p.Arg905Ter
XM_011532492.1:c.2779C>T	XP_011530794.1:p.Arg927Ter
XM_011532493.1:c.2641C>T	XP_011530795.1:p.Arg881Ter
XM_011532494.1:c.2581C>T	XP_011530796.1:p.Arg861Ter
XM_011532495.1:c.2113C>T	XP_011530797.1:p.Arg705Ter
XM_011532496.1:c.2056C>T	XP_011530798.1:p.Arg686Ter
NM_001320613.1:c.2656C>T	NP_001307542.1:p.Arg886Ter
NM_004036.4:c.2653C>T	NP_004027.2:p.Arg885Ter
XM_011532492.2:c.2779C>T	XP_011530794.1:p.Arg927Ter
XM_017003186.1:c.2719C>T	XP_016858675.1:p.Arg907Ter
XM_017003187.1:c.2710C>T	XP_016858676.1:p.Arg904Ter
XM_017003188.1:c.2776C>T	XP_016858677.1:p.Arg926Ter
XM_017003189.1:c.2638C>T	XP_016858678.1:p.Arg880Ter
XM_017003190.1:c.2515C>T	XP_016858679.1:p.Arg839Ter
XM_017003191.1:c.2143C>T	XP_016858680.1:p.Arg715Ter
XM_017003192.1:c.1933C>T	XP_016858681.1:p.Arg645Ter
XM_017003193.1:c.1930C>T	XP_016858682.1:p.Arg644Ter
NM_001320613.2:c.2656C>T	NP_001307542.1:p.Arg886Ter
NM_001377128.1:c.2719C>T	NP_001364057.1:p.Arg907Ter
NM_001377129.1:c.2515C>T	NP_001364058.1:p.Arg839Ter
NM_001377130.1:c.2248C>T	NP_001364059.1:p.Arg750Ter
NM_001377131.1:c.1930C>T	NP_001364060.1:p.Arg644Ter
NM_001377132.1:c.2653C>T	NP_001364061.1:p.Arg885Ter
NM_004036.5:c.2653C>T MANE Select	NP_004027.2:p.Arg885Ter