Canonical Allele Identifier: CA425172010

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046180G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823311G>C , CM000664.2:g.24823311G>C	GRCh38
NC_000002.11:g.25046180G>C , CM000664.1:g.25046180G>C	GRCh37
NC_000002.10:g.24899684G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2784C>G	ENSP00000384484.2:p.Ala928=
ENST00000679454.1:c.2781C>G MANE Select	ENSP00000505261.1:p.Ala927=
ENST00000260600.9:c.2781C>G	ENSP00000260600.5:p.Ala927=
ENST00000405392.5:c.2784C>G	ENSP00000384484.2:p.Ala928=
ENST00000485887.1:n.53C>G
ENST00000606682.5:c.1722C>G	ENSP00000475652.1:p.Ala574=
NM_004036.3:c.2781C>G	NP_004027.2:p.Ala927=
XM_005264104.1:c.2784C>G	XP_005264161.1:p.Ala928=
XM_005264105.1:c.2781C>G	XP_005264162.1:p.Ala927=
XM_006711925.1:c.2850C>G	XP_006711988.1:p.Ala950=
XM_011532489.1:c.2907C>G	XP_011530791.1:p.Ala969=
XM_011532490.1:c.2904C>G	XP_011530792.1:p.Ala968=
XM_011532491.1:c.2841C>G	XP_011530793.1:p.Ala947=
XM_011532492.1:c.2907C>G	XP_011530794.1:p.Ala969=
XM_011532493.1:c.2769C>G	XP_011530795.1:p.Ala923=
XM_011532494.1:c.2709C>G	XP_011530796.1:p.Ala903=
XM_011532495.1:c.2241C>G	XP_011530797.1:p.Ala747=
XM_011532496.1:c.2184C>G	XP_011530798.1:p.Ala728=
NM_001320613.1:c.2784C>G	NP_001307542.1:p.Ala928=
NM_004036.4:c.2781C>G	NP_004027.2:p.Ala927=
XM_011532492.2:c.2907C>G	XP_011530794.1:p.Ala969=
XM_017003186.1:c.2847C>G	XP_016858675.1:p.Ala949=
XM_017003187.1:c.2838C>G	XP_016858676.1:p.Ala946=
XM_017003188.1:c.2904C>G	XP_016858677.1:p.Ala968=
XM_017003189.1:c.2766C>G	XP_016858678.1:p.Ala922=
XM_017003190.1:c.2643C>G	XP_016858679.1:p.Ala881=
XM_017003191.1:c.2271C>G	XP_016858680.1:p.Ala757=
XM_017003192.1:c.2061C>G	XP_016858681.1:p.Ala687=
XM_017003193.1:c.2058C>G	XP_016858682.1:p.Ala686=
NM_001320613.2:c.2784C>G	NP_001307542.1:p.Ala928=
NM_001377128.1:c.2847C>G	NP_001364057.1:p.Ala949=
NM_001377129.1:c.2643C>G	NP_001364058.1:p.Ala881=
NM_001377130.1:c.2332-681C>G	NP_001364059.1:n.2332-681C>G
NM_001377131.1:c.2058C>G	NP_001364060.1:p.Ala686=
NM_001377132.1:c.2781C>G	NP_001364061.1:p.Ala927=
NM_004036.5:c.2781C>G MANE Select	NP_004027.2:p.Ala927=