Canonical Allele Identifier: CA346063649

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047326C>G (hg19) ; chr2:g.24824457C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824457C>G , CM000664.2:g.24824457C>G	GRCh38
NC_000002.11:g.25047326C>G , CM000664.1:g.25047326C>G	GRCh37
NC_000002.10:g.24900830C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2660G>C	ENSP00000384484.2:p.Arg887Pro
ENST00000679454.1:c.2657G>C MANE Select	ENSP00000505261.1:p.Arg886Pro
ENST00000260600.9:c.2657G>C	ENSP00000260600.5:p.Arg886Pro
ENST00000405392.5:c.2660G>C	ENSP00000384484.2:p.Arg887Pro
ENST00000606682.5:c.1598G>C	ENSP00000475652.1:p.Arg533Pro
NM_004036.3:c.2657G>C	NP_004027.2:p.Arg886Pro
XM_005264104.1:c.2660G>C	XP_005264161.1:p.Arg887Pro
XM_005264105.1:c.2657G>C	XP_005264162.1:p.Arg886Pro
XM_006711925.1:c.2726G>C	XP_006711988.1:p.Arg909Pro
XM_011532489.1:c.2783G>C	XP_011530791.1:p.Arg928Pro
XM_011532490.1:c.2780G>C	XP_011530792.1:p.Arg927Pro
XM_011532491.1:c.2717G>C	XP_011530793.1:p.Arg906Pro
XM_011532492.1:c.2783G>C	XP_011530794.1:p.Arg928Pro
XM_011532493.1:c.2645G>C	XP_011530795.1:p.Arg882Pro
XM_011532494.1:c.2585G>C	XP_011530796.1:p.Arg862Pro
XM_011532495.1:c.2117G>C	XP_011530797.1:p.Arg706Pro
XM_011532496.1:c.2060G>C	XP_011530798.1:p.Arg687Pro
NM_001320613.1:c.2660G>C	NP_001307542.1:p.Arg887Pro
NM_004036.4:c.2657G>C	NP_004027.2:p.Arg886Pro
XM_011532492.2:c.2783G>C	XP_011530794.1:p.Arg928Pro
XM_017003186.1:c.2723G>C	XP_016858675.1:p.Arg908Pro
XM_017003187.1:c.2714G>C	XP_016858676.1:p.Arg905Pro
XM_017003188.1:c.2780G>C	XP_016858677.1:p.Arg927Pro
XM_017003189.1:c.2642G>C	XP_016858678.1:p.Arg881Pro
XM_017003190.1:c.2519G>C	XP_016858679.1:p.Arg840Pro
XM_017003191.1:c.2147G>C	XP_016858680.1:p.Arg716Pro
XM_017003192.1:c.1937G>C	XP_016858681.1:p.Arg646Pro
XM_017003193.1:c.1934G>C	XP_016858682.1:p.Arg645Pro
NM_001320613.2:c.2660G>C	NP_001307542.1:p.Arg887Pro
NM_001377128.1:c.2723G>C	NP_001364057.1:p.Arg908Pro
NM_001377129.1:c.2519G>C	NP_001364058.1:p.Arg840Pro
NM_001377130.1:c.2252G>C	NP_001364059.1:p.Arg751Pro
NM_001377131.1:c.1934G>C	NP_001364060.1:p.Arg645Pro
NM_001377132.1:c.2657G>C	NP_001364061.1:p.Arg886Pro
NM_004036.5:c.2657G>C MANE Select	NP_004027.2:p.Arg886Pro