Canonical Allele Identifier: CA346063592

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047308A>G (hg19) ; chr2:g.24824439A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824439A>G , CM000664.2:g.24824439A>G	GRCh38
NC_000002.11:g.25047308A>G , CM000664.1:g.25047308A>G	GRCh37
NC_000002.10:g.24900812A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2678T>C	ENSP00000384484.2:p.Val893Ala
ENST00000679454.1:c.2675T>C MANE Select	ENSP00000505261.1:p.Val892Ala
ENST00000260600.9:c.2675T>C	ENSP00000260600.5:p.Val892Ala
ENST00000405392.5:c.2678T>C	ENSP00000384484.2:p.Val893Ala
ENST00000606682.5:c.1616T>C	ENSP00000475652.1:p.Val539Ala
NM_004036.3:c.2675T>C	NP_004027.2:p.Val892Ala
XM_005264104.1:c.2678T>C	XP_005264161.1:p.Val893Ala
XM_005264105.1:c.2675T>C	XP_005264162.1:p.Val892Ala
XM_006711925.1:c.2744T>C	XP_006711988.1:p.Val915Ala
XM_011532489.1:c.2801T>C	XP_011530791.1:p.Val934Ala
XM_011532490.1:c.2798T>C	XP_011530792.1:p.Val933Ala
XM_011532491.1:c.2735T>C	XP_011530793.1:p.Val912Ala
XM_011532492.1:c.2801T>C	XP_011530794.1:p.Val934Ala
XM_011532493.1:c.2663T>C	XP_011530795.1:p.Val888Ala
XM_011532494.1:c.2603T>C	XP_011530796.1:p.Val868Ala
XM_011532495.1:c.2135T>C	XP_011530797.1:p.Val712Ala
XM_011532496.1:c.2078T>C	XP_011530798.1:p.Val693Ala
NM_001320613.1:c.2678T>C	NP_001307542.1:p.Val893Ala
NM_004036.4:c.2675T>C	NP_004027.2:p.Val892Ala
XM_011532492.2:c.2801T>C	XP_011530794.1:p.Val934Ala
XM_017003186.1:c.2741T>C	XP_016858675.1:p.Val914Ala
XM_017003187.1:c.2732T>C	XP_016858676.1:p.Val911Ala
XM_017003188.1:c.2798T>C	XP_016858677.1:p.Val933Ala
XM_017003189.1:c.2660T>C	XP_016858678.1:p.Val887Ala
XM_017003190.1:c.2537T>C	XP_016858679.1:p.Val846Ala
XM_017003191.1:c.2165T>C	XP_016858680.1:p.Val722Ala
XM_017003192.1:c.1955T>C	XP_016858681.1:p.Val652Ala
XM_017003193.1:c.1952T>C	XP_016858682.1:p.Val651Ala
NM_001320613.2:c.2678T>C	NP_001307542.1:p.Val893Ala
NM_001377128.1:c.2741T>C	NP_001364057.1:p.Val914Ala
NM_001377129.1:c.2537T>C	NP_001364058.1:p.Val846Ala
NM_001377130.1:c.2270T>C	NP_001364059.1:p.Val757Ala
NM_001377131.1:c.1952T>C	NP_001364060.1:p.Val651Ala
NM_001377132.1:c.2675T>C	NP_001364061.1:p.Val892Ala
NM_004036.5:c.2675T>C MANE Select	NP_004027.2:p.Val892Ala