Canonical Allele Identifier: CA425172002

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046174C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823305C>A , CM000664.2:g.24823305C>A	GRCh38
NC_000002.11:g.25046174C>A , CM000664.1:g.25046174C>A	GRCh37
NC_000002.10:g.24899678C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2790G>T	ENSP00000384484.2:p.Leu930=
ENST00000679454.1:c.2787G>T MANE Select	ENSP00000505261.1:p.Leu929=
ENST00000260600.9:c.2787G>T	ENSP00000260600.5:p.Leu929=
ENST00000405392.5:c.2790G>T	ENSP00000384484.2:p.Leu930=
ENST00000485887.1:n.59G>T
ENST00000606682.5:c.1728G>T	ENSP00000475652.1:p.Leu576=
NM_004036.3:c.2787G>T	NP_004027.2:p.Leu929=
XM_005264104.1:c.2790G>T	XP_005264161.1:p.Leu930=
XM_005264105.1:c.2787G>T	XP_005264162.1:p.Leu929=
XM_006711925.1:c.2856G>T	XP_006711988.1:p.Leu952=
XM_011532489.1:c.2913G>T	XP_011530791.1:p.Leu971=
XM_011532490.1:c.2910G>T	XP_011530792.1:p.Leu970=
XM_011532491.1:c.2847G>T	XP_011530793.1:p.Leu949=
XM_011532492.1:c.2913G>T	XP_011530794.1:p.Leu971=
XM_011532493.1:c.2775G>T	XP_011530795.1:p.Leu925=
XM_011532494.1:c.2715G>T	XP_011530796.1:p.Leu905=
XM_011532495.1:c.2247G>T	XP_011530797.1:p.Leu749=
XM_011532496.1:c.2190G>T	XP_011530798.1:p.Leu730=
NM_001320613.1:c.2790G>T	NP_001307542.1:p.Leu930=
NM_004036.4:c.2787G>T	NP_004027.2:p.Leu929=
XM_011532492.2:c.2913G>T	XP_011530794.1:p.Leu971=
XM_017003186.1:c.2853G>T	XP_016858675.1:p.Leu951=
XM_017003187.1:c.2844G>T	XP_016858676.1:p.Leu948=
XM_017003188.1:c.2910G>T	XP_016858677.1:p.Leu970=
XM_017003189.1:c.2772G>T	XP_016858678.1:p.Leu924=
XM_017003190.1:c.2649G>T	XP_016858679.1:p.Leu883=
XM_017003191.1:c.2277G>T	XP_016858680.1:p.Leu759=
XM_017003192.1:c.2067G>T	XP_016858681.1:p.Leu689=
XM_017003193.1:c.2064G>T	XP_016858682.1:p.Leu688=
NM_001320613.2:c.2790G>T	NP_001307542.1:p.Leu930=
NM_001377128.1:c.2853G>T	NP_001364057.1:p.Leu951=
NM_001377129.1:c.2649G>T	NP_001364058.1:p.Leu883=
NM_001377130.1:c.2332-675G>T	NP_001364059.1:n.2332-675G>T
NM_001377131.1:c.2064G>T	NP_001364060.1:p.Leu688=
NM_001377132.1:c.2787G>T	NP_001364061.1:p.Leu929=
NM_004036.5:c.2787G>T MANE Select	NP_004027.2:p.Leu929=