Canonical Allele Identifier: CA346063588

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047306T>A (hg19) ; chr2:g.24824437T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824437T>A , CM000664.2:g.24824437T>A	GRCh38
NC_000002.11:g.25047306T>A , CM000664.1:g.25047306T>A	GRCh37
NC_000002.10:g.24900810T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2680A>T	ENSP00000384484.2:p.Thr894Ser
ENST00000679454.1:c.2677A>T MANE Select	ENSP00000505261.1:p.Thr893Ser
ENST00000260600.9:c.2677A>T	ENSP00000260600.5:p.Thr893Ser
ENST00000405392.5:c.2680A>T	ENSP00000384484.2:p.Thr894Ser
ENST00000606682.5:c.1618A>T	ENSP00000475652.1:p.Thr540Ser
NM_004036.3:c.2677A>T	NP_004027.2:p.Thr893Ser
XM_005264104.1:c.2680A>T	XP_005264161.1:p.Thr894Ser
XM_005264105.1:c.2677A>T	XP_005264162.1:p.Thr893Ser
XM_006711925.1:c.2746A>T	XP_006711988.1:p.Thr916Ser
XM_011532489.1:c.2803A>T	XP_011530791.1:p.Thr935Ser
XM_011532490.1:c.2800A>T	XP_011530792.1:p.Thr934Ser
XM_011532491.1:c.2737A>T	XP_011530793.1:p.Thr913Ser
XM_011532492.1:c.2803A>T	XP_011530794.1:p.Thr935Ser
XM_011532493.1:c.2665A>T	XP_011530795.1:p.Thr889Ser
XM_011532494.1:c.2605A>T	XP_011530796.1:p.Thr869Ser
XM_011532495.1:c.2137A>T	XP_011530797.1:p.Thr713Ser
XM_011532496.1:c.2080A>T	XP_011530798.1:p.Thr694Ser
NM_001320613.1:c.2680A>T	NP_001307542.1:p.Thr894Ser
NM_004036.4:c.2677A>T	NP_004027.2:p.Thr893Ser
XM_011532492.2:c.2803A>T	XP_011530794.1:p.Thr935Ser
XM_017003186.1:c.2743A>T	XP_016858675.1:p.Thr915Ser
XM_017003187.1:c.2734A>T	XP_016858676.1:p.Thr912Ser
XM_017003188.1:c.2800A>T	XP_016858677.1:p.Thr934Ser
XM_017003189.1:c.2662A>T	XP_016858678.1:p.Thr888Ser
XM_017003190.1:c.2539A>T	XP_016858679.1:p.Thr847Ser
XM_017003191.1:c.2167A>T	XP_016858680.1:p.Thr723Ser
XM_017003192.1:c.1957A>T	XP_016858681.1:p.Thr653Ser
XM_017003193.1:c.1954A>T	XP_016858682.1:p.Thr652Ser
NM_001320613.2:c.2680A>T	NP_001307542.1:p.Thr894Ser
NM_001377128.1:c.2743A>T	NP_001364057.1:p.Thr915Ser
NM_001377129.1:c.2539A>T	NP_001364058.1:p.Thr847Ser
NM_001377130.1:c.2272A>T	NP_001364059.1:p.Thr758Ser
NM_001377131.1:c.1954A>T	NP_001364060.1:p.Thr652Ser
NM_001377132.1:c.2677A>T	NP_001364061.1:p.Thr893Ser
NM_004036.5:c.2677A>T MANE Select	NP_004027.2:p.Thr893Ser