Canonical Allele Identifier: CA346063697

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047339A>C (hg19) ; chr2:g.24824470A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824470A>C , CM000664.2:g.24824470A>C	GRCh38
NC_000002.11:g.25047339A>C , CM000664.1:g.25047339A>C	GRCh37
NC_000002.10:g.24900843A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2647T>G	ENSP00000384484.2:p.Tyr883Asp
ENST00000679454.1:c.2644T>G MANE Select	ENSP00000505261.1:p.Tyr882Asp
ENST00000260600.9:c.2644T>G	ENSP00000260600.5:p.Tyr882Asp
ENST00000405392.5:c.2647T>G	ENSP00000384484.2:p.Tyr883Asp
ENST00000606682.5:c.1585T>G	ENSP00000475652.1:p.Tyr529Asp
NM_004036.3:c.2644T>G	NP_004027.2:p.Tyr882Asp
XM_005264104.1:c.2647T>G	XP_005264161.1:p.Tyr883Asp
XM_005264105.1:c.2644T>G	XP_005264162.1:p.Tyr882Asp
XM_006711925.1:c.2713T>G	XP_006711988.1:p.Tyr905Asp
XM_011532489.1:c.2770T>G	XP_011530791.1:p.Tyr924Asp
XM_011532490.1:c.2767T>G	XP_011530792.1:p.Tyr923Asp
XM_011532491.1:c.2704T>G	XP_011530793.1:p.Tyr902Asp
XM_011532492.1:c.2770T>G	XP_011530794.1:p.Tyr924Asp
XM_011532493.1:c.2632T>G	XP_011530795.1:p.Tyr878Asp
XM_011532494.1:c.2572T>G	XP_011530796.1:p.Tyr858Asp
XM_011532495.1:c.2104T>G	XP_011530797.1:p.Tyr702Asp
XM_011532496.1:c.2047T>G	XP_011530798.1:p.Tyr683Asp
NM_001320613.1:c.2647T>G	NP_001307542.1:p.Tyr883Asp
NM_004036.4:c.2644T>G	NP_004027.2:p.Tyr882Asp
XM_011532492.2:c.2770T>G	XP_011530794.1:p.Tyr924Asp
XM_017003186.1:c.2710T>G	XP_016858675.1:p.Tyr904Asp
XM_017003187.1:c.2701T>G	XP_016858676.1:p.Tyr901Asp
XM_017003188.1:c.2767T>G	XP_016858677.1:p.Tyr923Asp
XM_017003189.1:c.2629T>G	XP_016858678.1:p.Tyr877Asp
XM_017003190.1:c.2506T>G	XP_016858679.1:p.Tyr836Asp
XM_017003191.1:c.2134T>G	XP_016858680.1:p.Tyr712Asp
XM_017003192.1:c.1924T>G	XP_016858681.1:p.Tyr642Asp
XM_017003193.1:c.1921T>G	XP_016858682.1:p.Tyr641Asp
NM_001320613.2:c.2647T>G	NP_001307542.1:p.Tyr883Asp
NM_001377128.1:c.2710T>G	NP_001364057.1:p.Tyr904Asp
NM_001377129.1:c.2506T>G	NP_001364058.1:p.Tyr836Asp
NM_001377130.1:c.2239T>G	NP_001364059.1:p.Tyr747Asp
NM_001377131.1:c.1921T>G	NP_001364060.1:p.Tyr641Asp
NM_001377132.1:c.2644T>G	NP_001364061.1:p.Tyr882Asp
NM_004036.5:c.2644T>G MANE Select	NP_004027.2:p.Tyr882Asp