Canonical Allele Identifier: CA346062598

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046120C>G (hg19) ; chr2:g.24823251C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823251C>G , CM000664.2:g.24823251C>G	GRCh38
NC_000002.11:g.25046120C>G , CM000664.1:g.25046120C>G	GRCh37
NC_000002.10:g.24899624C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2844G>C	ENSP00000384484.2:p.Glu948Asp
ENST00000679454.1:c.2841G>C MANE Select	ENSP00000505261.1:p.Glu947Asp
ENST00000260600.9:c.2841G>C	ENSP00000260600.5:p.Glu947Asp
ENST00000405392.5:c.2844G>C	ENSP00000384484.2:p.Glu948Asp
ENST00000485887.1:n.113G>C
ENST00000606682.5:c.1782G>C	ENSP00000475652.1:p.Glu594Asp
NM_004036.3:c.2841G>C	NP_004027.2:p.Glu947Asp
XM_005264104.1:c.2844G>C	XP_005264161.1:p.Glu948Asp
XM_005264105.1:c.2841G>C	XP_005264162.1:p.Glu947Asp
XM_006711925.1:c.2910G>C	XP_006711988.1:p.Glu970Asp
XM_011532489.1:c.2967G>C	XP_011530791.1:p.Glu989Asp
XM_011532490.1:c.2964G>C	XP_011530792.1:p.Glu988Asp
XM_011532491.1:c.2901G>C	XP_011530793.1:p.Glu967Asp
XM_011532492.1:c.2967G>C	XP_011530794.1:p.Glu989Asp
XM_011532493.1:c.2829G>C	XP_011530795.1:p.Glu943Asp
XM_011532494.1:c.2769G>C	XP_011530796.1:p.Glu923Asp
XM_011532495.1:c.2301G>C	XP_011530797.1:p.Glu767Asp
XM_011532496.1:c.2244G>C	XP_011530798.1:p.Glu748Asp
NM_001320613.1:c.2844G>C	NP_001307542.1:p.Glu948Asp
NM_004036.4:c.2841G>C	NP_004027.2:p.Glu947Asp
XM_011532492.2:c.2967G>C	XP_011530794.1:p.Glu989Asp
XM_017003186.1:c.2907G>C	XP_016858675.1:p.Glu969Asp
XM_017003187.1:c.2898G>C	XP_016858676.1:p.Glu966Asp
XM_017003188.1:c.2964G>C	XP_016858677.1:p.Glu988Asp
XM_017003189.1:c.2826G>C	XP_016858678.1:p.Glu942Asp
XM_017003190.1:c.2703G>C	XP_016858679.1:p.Glu901Asp
XM_017003191.1:c.2331G>C	XP_016858680.1:p.Glu777Asp
XM_017003192.1:c.2121G>C	XP_016858681.1:p.Glu707Asp
XM_017003193.1:c.2118G>C	XP_016858682.1:p.Glu706Asp
NM_001320613.2:c.2844G>C	NP_001307542.1:p.Glu948Asp
NM_001377128.1:c.2907G>C	NP_001364057.1:p.Glu969Asp
NM_001377129.1:c.2703G>C	NP_001364058.1:p.Glu901Asp
NM_001377130.1:c.2332-621G>C	NP_001364059.1:n.2332-621G>C
NM_001377131.1:c.2118G>C	NP_001364060.1:p.Glu706Asp
NM_001377132.1:c.2841G>C	NP_001364061.1:p.Glu947Asp
NM_004036.5:c.2841G>C MANE Select	NP_004027.2:p.Glu947Asp