Canonical Allele Identifier: CA346062648

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046130C>G (hg19) ; chr2:g.24823261C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823261C>G , CM000664.2:g.24823261C>G	GRCh38
NC_000002.11:g.25046130C>G , CM000664.1:g.25046130C>G	GRCh37
NC_000002.10:g.24899634C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2834G>C	ENSP00000384484.2:p.Gly945Ala
ENST00000679454.1:c.2831G>C MANE Select	ENSP00000505261.1:p.Gly944Ala
ENST00000260600.9:c.2831G>C	ENSP00000260600.5:p.Gly944Ala
ENST00000405392.5:c.2834G>C	ENSP00000384484.2:p.Gly945Ala
ENST00000485887.1:n.103G>C
ENST00000606682.5:c.1772G>C	ENSP00000475652.1:p.Gly591Ala
NM_004036.3:c.2831G>C	NP_004027.2:p.Gly944Ala
XM_005264104.1:c.2834G>C	XP_005264161.1:p.Gly945Ala
XM_005264105.1:c.2831G>C	XP_005264162.1:p.Gly944Ala
XM_006711925.1:c.2900G>C	XP_006711988.1:p.Gly967Ala
XM_011532489.1:c.2957G>C	XP_011530791.1:p.Gly986Ala
XM_011532490.1:c.2954G>C	XP_011530792.1:p.Gly985Ala
XM_011532491.1:c.2891G>C	XP_011530793.1:p.Gly964Ala
XM_011532492.1:c.2957G>C	XP_011530794.1:p.Gly986Ala
XM_011532493.1:c.2819G>C	XP_011530795.1:p.Gly940Ala
XM_011532494.1:c.2759G>C	XP_011530796.1:p.Gly920Ala
XM_011532495.1:c.2291G>C	XP_011530797.1:p.Gly764Ala
XM_011532496.1:c.2234G>C	XP_011530798.1:p.Gly745Ala
NM_001320613.1:c.2834G>C	NP_001307542.1:p.Gly945Ala
NM_004036.4:c.2831G>C	NP_004027.2:p.Gly944Ala
XM_011532492.2:c.2957G>C	XP_011530794.1:p.Gly986Ala
XM_017003186.1:c.2897G>C	XP_016858675.1:p.Gly966Ala
XM_017003187.1:c.2888G>C	XP_016858676.1:p.Gly963Ala
XM_017003188.1:c.2954G>C	XP_016858677.1:p.Gly985Ala
XM_017003189.1:c.2816G>C	XP_016858678.1:p.Gly939Ala
XM_017003190.1:c.2693G>C	XP_016858679.1:p.Gly898Ala
XM_017003191.1:c.2321G>C	XP_016858680.1:p.Gly774Ala
XM_017003192.1:c.2111G>C	XP_016858681.1:p.Gly704Ala
XM_017003193.1:c.2108G>C	XP_016858682.1:p.Gly703Ala
NM_001320613.2:c.2834G>C	NP_001307542.1:p.Gly945Ala
NM_001377128.1:c.2897G>C	NP_001364057.1:p.Gly966Ala
NM_001377129.1:c.2693G>C	NP_001364058.1:p.Gly898Ala
NM_001377130.1:c.2332-631G>C	NP_001364059.1:n.2332-631G>C
NM_001377131.1:c.2108G>C	NP_001364060.1:p.Gly703Ala
NM_001377132.1:c.2831G>C	NP_001364061.1:p.Gly944Ala
NM_004036.5:c.2831G>C MANE Select	NP_004027.2:p.Gly944Ala