Canonical Allele Identifier: CA346062950

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046185A>C (hg19) ; chr2:g.24823316A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823316A>C , CM000664.2:g.24823316A>C	GRCh38
NC_000002.11:g.25046185A>C , CM000664.1:g.25046185A>C	GRCh37
NC_000002.10:g.24899689A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2779T>G	ENSP00000384484.2:p.Phe927Val
ENST00000679454.1:c.2776T>G MANE Select	ENSP00000505261.1:p.Phe926Val
ENST00000260600.9:c.2776T>G	ENSP00000260600.5:p.Phe926Val
ENST00000405392.5:c.2779T>G	ENSP00000384484.2:p.Phe927Val
ENST00000485887.1:n.48T>G
ENST00000606682.5:c.1717T>G	ENSP00000475652.1:p.Phe573Val
NM_004036.3:c.2776T>G	NP_004027.2:p.Phe926Val
XM_005264104.1:c.2779T>G	XP_005264161.1:p.Phe927Val
XM_005264105.1:c.2776T>G	XP_005264162.1:p.Phe926Val
XM_006711925.1:c.2845T>G	XP_006711988.1:p.Phe949Val
XM_011532489.1:c.2902T>G	XP_011530791.1:p.Phe968Val
XM_011532490.1:c.2899T>G	XP_011530792.1:p.Phe967Val
XM_011532491.1:c.2836T>G	XP_011530793.1:p.Phe946Val
XM_011532492.1:c.2902T>G	XP_011530794.1:p.Phe968Val
XM_011532493.1:c.2764T>G	XP_011530795.1:p.Phe922Val
XM_011532494.1:c.2704T>G	XP_011530796.1:p.Phe902Val
XM_011532495.1:c.2236T>G	XP_011530797.1:p.Phe746Val
XM_011532496.1:c.2179T>G	XP_011530798.1:p.Phe727Val
NM_001320613.1:c.2779T>G	NP_001307542.1:p.Phe927Val
NM_004036.4:c.2776T>G	NP_004027.2:p.Phe926Val
XM_011532492.2:c.2902T>G	XP_011530794.1:p.Phe968Val
XM_017003186.1:c.2842T>G	XP_016858675.1:p.Phe948Val
XM_017003187.1:c.2833T>G	XP_016858676.1:p.Phe945Val
XM_017003188.1:c.2899T>G	XP_016858677.1:p.Phe967Val
XM_017003189.1:c.2761T>G	XP_016858678.1:p.Phe921Val
XM_017003190.1:c.2638T>G	XP_016858679.1:p.Phe880Val
XM_017003191.1:c.2266T>G	XP_016858680.1:p.Phe756Val
XM_017003192.1:c.2056T>G	XP_016858681.1:p.Phe686Val
XM_017003193.1:c.2053T>G	XP_016858682.1:p.Phe685Val
NM_001320613.2:c.2779T>G	NP_001307542.1:p.Phe927Val
NM_001377128.1:c.2842T>G	NP_001364057.1:p.Phe948Val
NM_001377129.1:c.2638T>G	NP_001364058.1:p.Phe880Val
NM_001377130.1:c.2332-686T>G	NP_001364059.1:n.2332-686T>G
NM_001377131.1:c.2053T>G	NP_001364060.1:p.Phe685Val
NM_001377132.1:c.2776T>G	NP_001364061.1:p.Phe926Val
NM_004036.5:c.2776T>G MANE Select	NP_004027.2:p.Phe926Val