Canonical Allele Identifier: CA425172025

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046207C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823338C>A , CM000664.2:g.24823338C>A	GRCh38
NC_000002.11:g.25046207C>A , CM000664.1:g.25046207C>A	GRCh37
NC_000002.10:g.24899711C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2757G>T	ENSP00000384484.2:p.Thr919=
ENST00000679454.1:c.2754G>T MANE Select	ENSP00000505261.1:p.Thr918=
ENST00000260600.9:c.2754G>T	ENSP00000260600.5:p.Thr918=
ENST00000405392.5:c.2757G>T	ENSP00000384484.2:p.Thr919=
ENST00000485887.1:n.26G>T
ENST00000606682.5:c.1695G>T	ENSP00000475652.1:p.Thr565=
NM_004036.3:c.2754G>T	NP_004027.2:p.Thr918=
XM_005264104.1:c.2757G>T	XP_005264161.1:p.Thr919=
XM_005264105.1:c.2754G>T	XP_005264162.1:p.Thr918=
XM_006711925.1:c.2823G>T	XP_006711988.1:p.Thr941=
XM_011532489.1:c.2880G>T	XP_011530791.1:p.Thr960=
XM_011532490.1:c.2877G>T	XP_011530792.1:p.Thr959=
XM_011532491.1:c.2814G>T	XP_011530793.1:p.Thr938=
XM_011532492.1:c.2880G>T	XP_011530794.1:p.Thr960=
XM_011532493.1:c.2742G>T	XP_011530795.1:p.Thr914=
XM_011532494.1:c.2682G>T	XP_011530796.1:p.Thr894=
XM_011532495.1:c.2214G>T	XP_011530797.1:p.Thr738=
XM_011532496.1:c.2157G>T	XP_011530798.1:p.Thr719=
NM_001320613.1:c.2757G>T	NP_001307542.1:p.Thr919=
NM_004036.4:c.2754G>T	NP_004027.2:p.Thr918=
XM_011532492.2:c.2880G>T	XP_011530794.1:p.Thr960=
XM_017003186.1:c.2820G>T	XP_016858675.1:p.Thr940=
XM_017003187.1:c.2811G>T	XP_016858676.1:p.Thr937=
XM_017003188.1:c.2877G>T	XP_016858677.1:p.Thr959=
XM_017003189.1:c.2739G>T	XP_016858678.1:p.Thr913=
XM_017003190.1:c.2616G>T	XP_016858679.1:p.Thr872=
XM_017003191.1:c.2244G>T	XP_016858680.1:p.Thr748=
XM_017003192.1:c.2034G>T	XP_016858681.1:p.Thr678=
XM_017003193.1:c.2031G>T	XP_016858682.1:p.Thr677=
NM_001320613.2:c.2757G>T	NP_001307542.1:p.Thr919=
NM_001377128.1:c.2820G>T	NP_001364057.1:p.Thr940=
NM_001377129.1:c.2616G>T	NP_001364058.1:p.Thr872=
NM_001377130.1:c.2332-708G>T	NP_001364059.1:n.2332-708G>T
NM_001377131.1:c.2031G>T	NP_001364060.1:p.Thr677=
NM_001377132.1:c.2754G>T	NP_001364061.1:p.Thr918=
NM_004036.5:c.2754G>T MANE Select	NP_004027.2:p.Thr918=