Canonical Allele Identifier: CA425172017

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046192T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823323T>G , CM000664.2:g.24823323T>G	GRCh38
NC_000002.11:g.25046192T>G , CM000664.1:g.25046192T>G	GRCh37
NC_000002.10:g.24899696T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2772A>C	ENSP00000384484.2:p.Gly924=
ENST00000679454.1:c.2769A>C MANE Select	ENSP00000505261.1:p.Gly923=
ENST00000260600.9:c.2769A>C	ENSP00000260600.5:p.Gly923=
ENST00000405392.5:c.2772A>C	ENSP00000384484.2:p.Gly924=
ENST00000485887.1:n.41A>C
ENST00000606682.5:c.1710A>C	ENSP00000475652.1:p.Gly570=
NM_004036.3:c.2769A>C	NP_004027.2:p.Gly923=
XM_005264104.1:c.2772A>C	XP_005264161.1:p.Gly924=
XM_005264105.1:c.2769A>C	XP_005264162.1:p.Gly923=
XM_006711925.1:c.2838A>C	XP_006711988.1:p.Gly946=
XM_011532489.1:c.2895A>C	XP_011530791.1:p.Gly965=
XM_011532490.1:c.2892A>C	XP_011530792.1:p.Gly964=
XM_011532491.1:c.2829A>C	XP_011530793.1:p.Gly943=
XM_011532492.1:c.2895A>C	XP_011530794.1:p.Gly965=
XM_011532493.1:c.2757A>C	XP_011530795.1:p.Gly919=
XM_011532494.1:c.2697A>C	XP_011530796.1:p.Gly899=
XM_011532495.1:c.2229A>C	XP_011530797.1:p.Gly743=
XM_011532496.1:c.2172A>C	XP_011530798.1:p.Gly724=
NM_001320613.1:c.2772A>C	NP_001307542.1:p.Gly924=
NM_004036.4:c.2769A>C	NP_004027.2:p.Gly923=
XM_011532492.2:c.2895A>C	XP_011530794.1:p.Gly965=
XM_017003186.1:c.2835A>C	XP_016858675.1:p.Gly945=
XM_017003187.1:c.2826A>C	XP_016858676.1:p.Gly942=
XM_017003188.1:c.2892A>C	XP_016858677.1:p.Gly964=
XM_017003189.1:c.2754A>C	XP_016858678.1:p.Gly918=
XM_017003190.1:c.2631A>C	XP_016858679.1:p.Gly877=
XM_017003191.1:c.2259A>C	XP_016858680.1:p.Gly753=
XM_017003192.1:c.2049A>C	XP_016858681.1:p.Gly683=
XM_017003193.1:c.2046A>C	XP_016858682.1:p.Gly682=
NM_001320613.2:c.2772A>C	NP_001307542.1:p.Gly924=
NM_001377128.1:c.2835A>C	NP_001364057.1:p.Gly945=
NM_001377129.1:c.2631A>C	NP_001364058.1:p.Gly877=
NM_001377130.1:c.2332-693A>C	NP_001364059.1:n.2332-693A>C
NM_001377131.1:c.2046A>C	NP_001364060.1:p.Gly682=
NM_001377132.1:c.2769A>C	NP_001364061.1:p.Gly923=
NM_004036.5:c.2769A>C MANE Select	NP_004027.2:p.Gly923=