Canonical Allele Identifier: CA346062635

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046127C>T (hg19) ; chr2:g.24823258C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823258C>T , CM000664.2:g.24823258C>T	GRCh38
NC_000002.11:g.25046127C>T , CM000664.1:g.25046127C>T	GRCh37
NC_000002.10:g.24899631C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2837G>A	ENSP00000384484.2:p.Gly946Asp
ENST00000679454.1:c.2834G>A MANE Select	ENSP00000505261.1:p.Gly945Asp
ENST00000260600.9:c.2834G>A	ENSP00000260600.5:p.Gly945Asp
ENST00000405392.5:c.2837G>A	ENSP00000384484.2:p.Gly946Asp
ENST00000485887.1:n.106G>A
ENST00000606682.5:c.1775G>A	ENSP00000475652.1:p.Gly592Asp
NM_004036.3:c.2834G>A	NP_004027.2:p.Gly945Asp
XM_005264104.1:c.2837G>A	XP_005264161.1:p.Gly946Asp
XM_005264105.1:c.2834G>A	XP_005264162.1:p.Gly945Asp
XM_006711925.1:c.2903G>A	XP_006711988.1:p.Gly968Asp
XM_011532489.1:c.2960G>A	XP_011530791.1:p.Gly987Asp
XM_011532490.1:c.2957G>A	XP_011530792.1:p.Gly986Asp
XM_011532491.1:c.2894G>A	XP_011530793.1:p.Gly965Asp
XM_011532492.1:c.2960G>A	XP_011530794.1:p.Gly987Asp
XM_011532493.1:c.2822G>A	XP_011530795.1:p.Gly941Asp
XM_011532494.1:c.2762G>A	XP_011530796.1:p.Gly921Asp
XM_011532495.1:c.2294G>A	XP_011530797.1:p.Gly765Asp
XM_011532496.1:c.2237G>A	XP_011530798.1:p.Gly746Asp
NM_001320613.1:c.2837G>A	NP_001307542.1:p.Gly946Asp
NM_004036.4:c.2834G>A	NP_004027.2:p.Gly945Asp
XM_011532492.2:c.2960G>A	XP_011530794.1:p.Gly987Asp
XM_017003186.1:c.2900G>A	XP_016858675.1:p.Gly967Asp
XM_017003187.1:c.2891G>A	XP_016858676.1:p.Gly964Asp
XM_017003188.1:c.2957G>A	XP_016858677.1:p.Gly986Asp
XM_017003189.1:c.2819G>A	XP_016858678.1:p.Gly940Asp
XM_017003190.1:c.2696G>A	XP_016858679.1:p.Gly899Asp
XM_017003191.1:c.2324G>A	XP_016858680.1:p.Gly775Asp
XM_017003192.1:c.2114G>A	XP_016858681.1:p.Gly705Asp
XM_017003193.1:c.2111G>A	XP_016858682.1:p.Gly704Asp
NM_001320613.2:c.2837G>A	NP_001307542.1:p.Gly946Asp
NM_001377128.1:c.2900G>A	NP_001364057.1:p.Gly967Asp
NM_001377129.1:c.2696G>A	NP_001364058.1:p.Gly899Asp
NM_001377130.1:c.2332-628G>A	NP_001364059.1:n.2332-628G>A
NM_001377131.1:c.2111G>A	NP_001364060.1:p.Gly704Asp
NM_001377132.1:c.2834G>A	NP_001364061.1:p.Gly945Asp
NM_004036.5:c.2834G>A MANE Select	NP_004027.2:p.Gly945Asp