Canonical Allele Identifier: CA346063523

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047291C>G (hg19) ; chr2:g.24824422C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824422C>G , CM000664.2:g.24824422C>G	GRCh38
NC_000002.11:g.25047291C>G , CM000664.1:g.25047291C>G	GRCh37
NC_000002.10:g.24900795C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2695G>C	ENSP00000384484.2:p.Glu899Gln
ENST00000679454.1:c.2692G>C MANE Select	ENSP00000505261.1:p.Glu898Gln
ENST00000260600.9:c.2692G>C	ENSP00000260600.5:p.Glu898Gln
ENST00000405392.5:c.2695G>C	ENSP00000384484.2:p.Glu899Gln
ENST00000606682.5:c.1633G>C	ENSP00000475652.1:p.Glu545Gln
NM_004036.3:c.2692G>C	NP_004027.2:p.Glu898Gln
XM_005264104.1:c.2695G>C	XP_005264161.1:p.Glu899Gln
XM_005264105.1:c.2692G>C	XP_005264162.1:p.Glu898Gln
XM_006711925.1:c.2761G>C	XP_006711988.1:p.Glu921Gln
XM_011532489.1:c.2818G>C	XP_011530791.1:p.Glu940Gln
XM_011532490.1:c.2815G>C	XP_011530792.1:p.Glu939Gln
XM_011532491.1:c.2752G>C	XP_011530793.1:p.Glu918Gln
XM_011532492.1:c.2818G>C	XP_011530794.1:p.Glu940Gln
XM_011532493.1:c.2680G>C	XP_011530795.1:p.Glu894Gln
XM_011532494.1:c.2620G>C	XP_011530796.1:p.Glu874Gln
XM_011532495.1:c.2152G>C	XP_011530797.1:p.Glu718Gln
XM_011532496.1:c.2095G>C	XP_011530798.1:p.Glu699Gln
NM_001320613.1:c.2695G>C	NP_001307542.1:p.Glu899Gln
NM_004036.4:c.2692G>C	NP_004027.2:p.Glu898Gln
XM_011532492.2:c.2818G>C	XP_011530794.1:p.Glu940Gln
XM_017003186.1:c.2758G>C	XP_016858675.1:p.Glu920Gln
XM_017003187.1:c.2749G>C	XP_016858676.1:p.Glu917Gln
XM_017003188.1:c.2815G>C	XP_016858677.1:p.Glu939Gln
XM_017003189.1:c.2677G>C	XP_016858678.1:p.Glu893Gln
XM_017003190.1:c.2554G>C	XP_016858679.1:p.Glu852Gln
XM_017003191.1:c.2182G>C	XP_016858680.1:p.Glu728Gln
XM_017003192.1:c.1972G>C	XP_016858681.1:p.Glu658Gln
XM_017003193.1:c.1969G>C	XP_016858682.1:p.Glu657Gln
NM_001320613.2:c.2695G>C	NP_001307542.1:p.Glu899Gln
NM_001377128.1:c.2758G>C	NP_001364057.1:p.Glu920Gln
NM_001377129.1:c.2554G>C	NP_001364058.1:p.Glu852Gln
NM_001377130.1:c.2287G>C	NP_001364059.1:p.Glu763Gln
NM_001377131.1:c.1969G>C	NP_001364060.1:p.Glu657Gln
NM_001377132.1:c.2692G>C	NP_001364061.1:p.Glu898Gln
NM_004036.5:c.2692G>C MANE Select	NP_004027.2:p.Glu898Gln