Canonical Allele Identifier: CA346063749

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047354G>C (hg19) ; chr2:g.24824485G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824485G>C , CM000664.2:g.24824485G>C	GRCh38
NC_000002.11:g.25047354G>C , CM000664.1:g.25047354G>C	GRCh37
NC_000002.10:g.24900858G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2632C>G	ENSP00000384484.2:p.Gln878Glu
ENST00000679454.1:c.2629C>G MANE Select	ENSP00000505261.1:p.Gln877Glu
ENST00000260600.9:c.2629C>G	ENSP00000260600.5:p.Gln877Glu
ENST00000405392.5:c.2632C>G	ENSP00000384484.2:p.Gln878Glu
ENST00000606682.5:c.1570C>G	ENSP00000475652.1:p.Gln524Glu
NM_004036.3:c.2629C>G	NP_004027.2:p.Gln877Glu
XM_005264104.1:c.2632C>G	XP_005264161.1:p.Gln878Glu
XM_005264105.1:c.2629C>G	XP_005264162.1:p.Gln877Glu
XM_006711925.1:c.2698C>G	XP_006711988.1:p.Gln900Glu
XM_011532489.1:c.2755C>G	XP_011530791.1:p.Gln919Glu
XM_011532490.1:c.2752C>G	XP_011530792.1:p.Gln918Glu
XM_011532491.1:c.2689C>G	XP_011530793.1:p.Gln897Glu
XM_011532492.1:c.2755C>G	XP_011530794.1:p.Gln919Glu
XM_011532493.1:c.2617C>G	XP_011530795.1:p.Gln873Glu
XM_011532494.1:c.2557C>G	XP_011530796.1:p.Gln853Glu
XM_011532495.1:c.2089C>G	XP_011530797.1:p.Gln697Glu
XM_011532496.1:c.2032C>G	XP_011530798.1:p.Gln678Glu
NM_001320613.1:c.2632C>G	NP_001307542.1:p.Gln878Glu
NM_004036.4:c.2629C>G	NP_004027.2:p.Gln877Glu
XM_011532492.2:c.2755C>G	XP_011530794.1:p.Gln919Glu
XM_017003186.1:c.2695C>G	XP_016858675.1:p.Gln899Glu
XM_017003187.1:c.2686C>G	XP_016858676.1:p.Gln896Glu
XM_017003188.1:c.2752C>G	XP_016858677.1:p.Gln918Glu
XM_017003189.1:c.2614C>G	XP_016858678.1:p.Gln872Glu
XM_017003190.1:c.2491C>G	XP_016858679.1:p.Gln831Glu
XM_017003191.1:c.2119C>G	XP_016858680.1:p.Gln707Glu
XM_017003192.1:c.1909C>G	XP_016858681.1:p.Gln637Glu
XM_017003193.1:c.1906C>G	XP_016858682.1:p.Gln636Glu
NM_001320613.2:c.2632C>G	NP_001307542.1:p.Gln878Glu
NM_001377128.1:c.2695C>G	NP_001364057.1:p.Gln899Glu
NM_001377129.1:c.2491C>G	NP_001364058.1:p.Gln831Glu
NM_001377130.1:c.2224C>G	NP_001364059.1:p.Gln742Glu
NM_001377131.1:c.1906C>G	NP_001364060.1:p.Gln636Glu
NM_001377132.1:c.2629C>G	NP_001364061.1:p.Gln877Glu
NM_004036.5:c.2629C>G MANE Select	NP_004027.2:p.Gln877Glu