Canonical Allele Identifier: CA346062975

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046190A>T (hg19) ; chr2:g.24823321A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823321A>T , CM000664.2:g.24823321A>T	GRCh38
NC_000002.11:g.25046190A>T , CM000664.1:g.25046190A>T	GRCh37
NC_000002.10:g.24899694A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2774T>A	ENSP00000384484.2:p.Val925Asp
ENST00000679454.1:c.2771T>A MANE Select	ENSP00000505261.1:p.Val924Asp
ENST00000260600.9:c.2771T>A	ENSP00000260600.5:p.Val924Asp
ENST00000405392.5:c.2774T>A	ENSP00000384484.2:p.Val925Asp
ENST00000485887.1:n.43T>A
ENST00000606682.5:c.1712T>A	ENSP00000475652.1:p.Val571Asp
NM_004036.3:c.2771T>A	NP_004027.2:p.Val924Asp
XM_005264104.1:c.2774T>A	XP_005264161.1:p.Val925Asp
XM_005264105.1:c.2771T>A	XP_005264162.1:p.Val924Asp
XM_006711925.1:c.2840T>A	XP_006711988.1:p.Val947Asp
XM_011532489.1:c.2897T>A	XP_011530791.1:p.Val966Asp
XM_011532490.1:c.2894T>A	XP_011530792.1:p.Val965Asp
XM_011532491.1:c.2831T>A	XP_011530793.1:p.Val944Asp
XM_011532492.1:c.2897T>A	XP_011530794.1:p.Val966Asp
XM_011532493.1:c.2759T>A	XP_011530795.1:p.Val920Asp
XM_011532494.1:c.2699T>A	XP_011530796.1:p.Val900Asp
XM_011532495.1:c.2231T>A	XP_011530797.1:p.Val744Asp
XM_011532496.1:c.2174T>A	XP_011530798.1:p.Val725Asp
NM_001320613.1:c.2774T>A	NP_001307542.1:p.Val925Asp
NM_004036.4:c.2771T>A	NP_004027.2:p.Val924Asp
XM_011532492.2:c.2897T>A	XP_011530794.1:p.Val966Asp
XM_017003186.1:c.2837T>A	XP_016858675.1:p.Val946Asp
XM_017003187.1:c.2828T>A	XP_016858676.1:p.Val943Asp
XM_017003188.1:c.2894T>A	XP_016858677.1:p.Val965Asp
XM_017003189.1:c.2756T>A	XP_016858678.1:p.Val919Asp
XM_017003190.1:c.2633T>A	XP_016858679.1:p.Val878Asp
XM_017003191.1:c.2261T>A	XP_016858680.1:p.Val754Asp
XM_017003192.1:c.2051T>A	XP_016858681.1:p.Val684Asp
XM_017003193.1:c.2048T>A	XP_016858682.1:p.Val683Asp
NM_001320613.2:c.2774T>A	NP_001307542.1:p.Val925Asp
NM_001377128.1:c.2837T>A	NP_001364057.1:p.Val946Asp
NM_001377129.1:c.2633T>A	NP_001364058.1:p.Val878Asp
NM_001377130.1:c.2332-691T>A	NP_001364059.1:n.2332-691T>A
NM_001377131.1:c.2048T>A	NP_001364060.1:p.Val683Asp
NM_001377132.1:c.2771T>A	NP_001364061.1:p.Val924Asp
NM_004036.5:c.2771T>A MANE Select	NP_004027.2:p.Val924Asp