Canonical Allele Identifier: CA425171996

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046162A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823293A>T , CM000664.2:g.24823293A>T	GRCh38
NC_000002.11:g.25046162A>T , CM000664.1:g.25046162A>T	GRCh37
NC_000002.10:g.24899666A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2802T>A	ENSP00000384484.2:p.Ala934=
ENST00000679454.1:c.2799T>A MANE Select	ENSP00000505261.1:p.Ala933=
ENST00000260600.9:c.2799T>A	ENSP00000260600.5:p.Ala933=
ENST00000405392.5:c.2802T>A	ENSP00000384484.2:p.Ala934=
ENST00000485887.1:n.71T>A
ENST00000606682.5:c.1740T>A	ENSP00000475652.1:p.Ala580=
NM_004036.3:c.2799T>A	NP_004027.2:p.Ala933=
XM_005264104.1:c.2802T>A	XP_005264161.1:p.Ala934=
XM_005264105.1:c.2799T>A	XP_005264162.1:p.Ala933=
XM_006711925.1:c.2868T>A	XP_006711988.1:p.Ala956=
XM_011532489.1:c.2925T>A	XP_011530791.1:p.Ala975=
XM_011532490.1:c.2922T>A	XP_011530792.1:p.Ala974=
XM_011532491.1:c.2859T>A	XP_011530793.1:p.Ala953=
XM_011532492.1:c.2925T>A	XP_011530794.1:p.Ala975=
XM_011532493.1:c.2787T>A	XP_011530795.1:p.Ala929=
XM_011532494.1:c.2727T>A	XP_011530796.1:p.Ala909=
XM_011532495.1:c.2259T>A	XP_011530797.1:p.Ala753=
XM_011532496.1:c.2202T>A	XP_011530798.1:p.Ala734=
NM_001320613.1:c.2802T>A	NP_001307542.1:p.Ala934=
NM_004036.4:c.2799T>A	NP_004027.2:p.Ala933=
XM_011532492.2:c.2925T>A	XP_011530794.1:p.Ala975=
XM_017003186.1:c.2865T>A	XP_016858675.1:p.Ala955=
XM_017003187.1:c.2856T>A	XP_016858676.1:p.Ala952=
XM_017003188.1:c.2922T>A	XP_016858677.1:p.Ala974=
XM_017003189.1:c.2784T>A	XP_016858678.1:p.Ala928=
XM_017003190.1:c.2661T>A	XP_016858679.1:p.Ala887=
XM_017003191.1:c.2289T>A	XP_016858680.1:p.Ala763=
XM_017003192.1:c.2079T>A	XP_016858681.1:p.Ala693=
XM_017003193.1:c.2076T>A	XP_016858682.1:p.Ala692=
NM_001320613.2:c.2802T>A	NP_001307542.1:p.Ala934=
NM_001377128.1:c.2865T>A	NP_001364057.1:p.Ala955=
NM_001377129.1:c.2661T>A	NP_001364058.1:p.Ala887=
NM_001377130.1:c.2332-663T>A	NP_001364059.1:n.2332-663T>A
NM_001377131.1:c.2076T>A	NP_001364060.1:p.Ala692=
NM_001377132.1:c.2799T>A	NP_001364061.1:p.Ala933=
NM_004036.5:c.2799T>A MANE Select	NP_004027.2:p.Ala933=