Canonical Allele Identifier: CA425172019

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046195A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823326A>G , CM000664.2:g.24823326A>G	GRCh38
NC_000002.11:g.25046195A>G , CM000664.1:g.25046195A>G	GRCh37
NC_000002.10:g.24899699A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2769T>C	ENSP00000384484.2:p.Ile923=
ENST00000679454.1:c.2766T>C MANE Select	ENSP00000505261.1:p.Ile922=
ENST00000260600.9:c.2766T>C	ENSP00000260600.5:p.Ile922=
ENST00000405392.5:c.2769T>C	ENSP00000384484.2:p.Ile923=
ENST00000485887.1:n.38T>C
ENST00000606682.5:c.1707T>C	ENSP00000475652.1:p.Ile569=
NM_004036.3:c.2766T>C	NP_004027.2:p.Ile922=
XM_005264104.1:c.2769T>C	XP_005264161.1:p.Ile923=
XM_005264105.1:c.2766T>C	XP_005264162.1:p.Ile922=
XM_006711925.1:c.2835T>C	XP_006711988.1:p.Ile945=
XM_011532489.1:c.2892T>C	XP_011530791.1:p.Ile964=
XM_011532490.1:c.2889T>C	XP_011530792.1:p.Ile963=
XM_011532491.1:c.2826T>C	XP_011530793.1:p.Ile942=
XM_011532492.1:c.2892T>C	XP_011530794.1:p.Ile964=
XM_011532493.1:c.2754T>C	XP_011530795.1:p.Ile918=
XM_011532494.1:c.2694T>C	XP_011530796.1:p.Ile898=
XM_011532495.1:c.2226T>C	XP_011530797.1:p.Ile742=
XM_011532496.1:c.2169T>C	XP_011530798.1:p.Ile723=
NM_001320613.1:c.2769T>C	NP_001307542.1:p.Ile923=
NM_004036.4:c.2766T>C	NP_004027.2:p.Ile922=
XM_011532492.2:c.2892T>C	XP_011530794.1:p.Ile964=
XM_017003186.1:c.2832T>C	XP_016858675.1:p.Ile944=
XM_017003187.1:c.2823T>C	XP_016858676.1:p.Ile941=
XM_017003188.1:c.2889T>C	XP_016858677.1:p.Ile963=
XM_017003189.1:c.2751T>C	XP_016858678.1:p.Ile917=
XM_017003190.1:c.2628T>C	XP_016858679.1:p.Ile876=
XM_017003191.1:c.2256T>C	XP_016858680.1:p.Ile752=
XM_017003192.1:c.2046T>C	XP_016858681.1:p.Ile682=
XM_017003193.1:c.2043T>C	XP_016858682.1:p.Ile681=
NM_001320613.2:c.2769T>C	NP_001307542.1:p.Ile923=
NM_001377128.1:c.2832T>C	NP_001364057.1:p.Ile944=
NM_001377129.1:c.2628T>C	NP_001364058.1:p.Ile876=
NM_001377130.1:c.2332-696T>C	NP_001364059.1:n.2332-696T>C
NM_001377131.1:c.2043T>C	NP_001364060.1:p.Ile681=
NM_001377132.1:c.2766T>C	NP_001364061.1:p.Ile922=
NM_004036.5:c.2766T>C MANE Select	NP_004027.2:p.Ile922=