Canonical Allele Identifier: CA346062645

Gene: ADCY3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2834G>T	ENSP00000384484.2:p.Gly945Val
ENST00000679454.1:c.2831G>T MANE Select	ENSP00000505261.1:p.Gly944Val
ENST00000260600.9:c.2831G>T	ENSP00000260600.5:p.Gly944Val
ENST00000405392.5:c.2834G>T	ENSP00000384484.2:p.Gly945Val
ENST00000485887.1:n.103G>T
ENST00000606682.5:c.1772G>T	ENSP00000475652.1:p.Gly591Val
NM_004036.3:c.2831G>T	NP_004027.2:p.Gly944Val
XM_005264104.1:c.2834G>T	XP_005264161.1:p.Gly945Val
XM_005264105.1:c.2831G>T	XP_005264162.1:p.Gly944Val
XM_006711925.1:c.2900G>T	XP_006711988.1:p.Gly967Val
XM_011532489.1:c.2957G>T	XP_011530791.1:p.Gly986Val
XM_011532490.1:c.2954G>T	XP_011530792.1:p.Gly985Val
XM_011532491.1:c.2891G>T	XP_011530793.1:p.Gly964Val
XM_011532492.1:c.2957G>T	XP_011530794.1:p.Gly986Val
XM_011532493.1:c.2819G>T	XP_011530795.1:p.Gly940Val
XM_011532494.1:c.2759G>T	XP_011530796.1:p.Gly920Val
XM_011532495.1:c.2291G>T	XP_011530797.1:p.Gly764Val
XM_011532496.1:c.2234G>T	XP_011530798.1:p.Gly745Val
NM_001320613.1:c.2834G>T	NP_001307542.1:p.Gly945Val
NM_004036.4:c.2831G>T	NP_004027.2:p.Gly944Val
XM_011532492.2:c.2957G>T	XP_011530794.1:p.Gly986Val
XM_017003186.1:c.2897G>T	XP_016858675.1:p.Gly966Val
XM_017003187.1:c.2888G>T	XP_016858676.1:p.Gly963Val
XM_017003188.1:c.2954G>T	XP_016858677.1:p.Gly985Val
XM_017003189.1:c.2816G>T	XP_016858678.1:p.Gly939Val
XM_017003190.1:c.2693G>T	XP_016858679.1:p.Gly898Val
XM_017003191.1:c.2321G>T	XP_016858680.1:p.Gly774Val
XM_017003192.1:c.2111G>T	XP_016858681.1:p.Gly704Val
XM_017003193.1:c.2108G>T	XP_016858682.1:p.Gly703Val
NM_001320613.2:c.2834G>T	NP_001307542.1:p.Gly945Val
NM_001377128.1:c.2897G>T	NP_001364057.1:p.Gly966Val
NM_001377129.1:c.2693G>T	NP_001364058.1:p.Gly898Val
NM_001377130.1:c.2332-631G>T	NP_001364059.1:n.2332-631G>T
NM_001377131.1:c.2108G>T	NP_001364060.1:p.Gly703Val
NM_001377132.1:c.2831G>T	NP_001364061.1:p.Gly944Val
NM_004036.5:c.2831G>T MANE Select	NP_004027.2:p.Gly944Val