Canonical Allele Identifier: CA425172165

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047304G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824435G>T , CM000664.2:g.24824435G>T	GRCh38
NC_000002.11:g.25047304G>T , CM000664.1:g.25047304G>T	GRCh37
NC_000002.10:g.24900808G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2682C>A	ENSP00000384484.2:p.Thr894=
ENST00000679454.1:c.2679C>A MANE Select	ENSP00000505261.1:p.Thr893=
ENST00000260600.9:c.2679C>A	ENSP00000260600.5:p.Thr893=
ENST00000405392.5:c.2682C>A	ENSP00000384484.2:p.Thr894=
ENST00000606682.5:c.1620C>A	ENSP00000475652.1:p.Thr540=
NM_004036.3:c.2679C>A	NP_004027.2:p.Thr893=
XM_005264104.1:c.2682C>A	XP_005264161.1:p.Thr894=
XM_005264105.1:c.2679C>A	XP_005264162.1:p.Thr893=
XM_006711925.1:c.2748C>A	XP_006711988.1:p.Thr916=
XM_011532489.1:c.2805C>A	XP_011530791.1:p.Thr935=
XM_011532490.1:c.2802C>A	XP_011530792.1:p.Thr934=
XM_011532491.1:c.2739C>A	XP_011530793.1:p.Thr913=
XM_011532492.1:c.2805C>A	XP_011530794.1:p.Thr935=
XM_011532493.1:c.2667C>A	XP_011530795.1:p.Thr889=
XM_011532494.1:c.2607C>A	XP_011530796.1:p.Thr869=
XM_011532495.1:c.2139C>A	XP_011530797.1:p.Thr713=
XM_011532496.1:c.2082C>A	XP_011530798.1:p.Thr694=
NM_001320613.1:c.2682C>A	NP_001307542.1:p.Thr894=
NM_004036.4:c.2679C>A	NP_004027.2:p.Thr893=
XM_011532492.2:c.2805C>A	XP_011530794.1:p.Thr935=
XM_017003186.1:c.2745C>A	XP_016858675.1:p.Thr915=
XM_017003187.1:c.2736C>A	XP_016858676.1:p.Thr912=
XM_017003188.1:c.2802C>A	XP_016858677.1:p.Thr934=
XM_017003189.1:c.2664C>A	XP_016858678.1:p.Thr888=
XM_017003190.1:c.2541C>A	XP_016858679.1:p.Thr847=
XM_017003191.1:c.2169C>A	XP_016858680.1:p.Thr723=
XM_017003192.1:c.1959C>A	XP_016858681.1:p.Thr653=
XM_017003193.1:c.1956C>A	XP_016858682.1:p.Thr652=
NM_001320613.2:c.2682C>A	NP_001307542.1:p.Thr894=
NM_001377128.1:c.2745C>A	NP_001364057.1:p.Thr915=
NM_001377129.1:c.2541C>A	NP_001364058.1:p.Thr847=
NM_001377130.1:c.2274C>A	NP_001364059.1:p.Thr758=
NM_001377131.1:c.1956C>A	NP_001364060.1:p.Thr652=
NM_001377132.1:c.2679C>A	NP_001364061.1:p.Thr893=
NM_004036.5:c.2679C>A MANE Select	NP_004027.2:p.Thr893=