Canonical Allele Identifier: CA43683271

Gene: ADCY3

Linked Data

• dbSNP Id: rs1031082505
• gnomAD v2: 2-25047319-G-A
• gnomAD v4: 2-24824450-G-A
• MyVariant Identifiers: chr2:g.25047319G>A (hg19) ; chr2:g.24824450G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824450G>A , CM000664.2:g.24824450G>A	GRCh38
NC_000002.11:g.25047319G>A , CM000664.1:g.25047319G>A	GRCh37
NC_000002.10:g.24900823G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2667C>T	ENSP00000384484.2:p.Asn889=
ENST00000679454.1:c.2664C>T MANE Select	ENSP00000505261.1:p.Asn888=
ENST00000260600.9:c.2664C>T	ENSP00000260600.5:p.Asn888=
ENST00000405392.5:c.2667C>T	ENSP00000384484.2:p.Asn889=
ENST00000606682.5:c.1605C>T	ENSP00000475652.1:p.Asn535=
NM_004036.3:c.2664C>T	NP_004027.2:p.Asn888=
XM_005264104.1:c.2667C>T	XP_005264161.1:p.Asn889=
XM_005264105.1:c.2664C>T	XP_005264162.1:p.Asn888=
XM_006711925.1:c.2733C>T	XP_006711988.1:p.Asn911=
XM_011532489.1:c.2790C>T	XP_011530791.1:p.Asn930=
XM_011532490.1:c.2787C>T	XP_011530792.1:p.Asn929=
XM_011532491.1:c.2724C>T	XP_011530793.1:p.Asn908=
XM_011532492.1:c.2790C>T	XP_011530794.1:p.Asn930=
XM_011532493.1:c.2652C>T	XP_011530795.1:p.Asn884=
XM_011532494.1:c.2592C>T	XP_011530796.1:p.Asn864=
XM_011532495.1:c.2124C>T	XP_011530797.1:p.Asn708=
XM_011532496.1:c.2067C>T	XP_011530798.1:p.Asn689=
NM_001320613.1:c.2667C>T	NP_001307542.1:p.Asn889=
NM_004036.4:c.2664C>T	NP_004027.2:p.Asn888=
XM_011532492.2:c.2790C>T	XP_011530794.1:p.Asn930=
XM_017003186.1:c.2730C>T	XP_016858675.1:p.Asn910=
XM_017003187.1:c.2721C>T	XP_016858676.1:p.Asn907=
XM_017003188.1:c.2787C>T	XP_016858677.1:p.Asn929=
XM_017003189.1:c.2649C>T	XP_016858678.1:p.Asn883=
XM_017003190.1:c.2526C>T	XP_016858679.1:p.Asn842=
XM_017003191.1:c.2154C>T	XP_016858680.1:p.Asn718=
XM_017003192.1:c.1944C>T	XP_016858681.1:p.Asn648=
XM_017003193.1:c.1941C>T	XP_016858682.1:p.Asn647=
NM_001320613.2:c.2667C>T	NP_001307542.1:p.Asn889=
NM_001377128.1:c.2730C>T	NP_001364057.1:p.Asn910=
NM_001377129.1:c.2526C>T	NP_001364058.1:p.Asn842=
NM_001377130.1:c.2259C>T	NP_001364059.1:p.Asn753=
NM_001377131.1:c.1941C>T	NP_001364060.1:p.Asn647=
NM_001377132.1:c.2664C>T	NP_001364061.1:p.Asn888=
NM_004036.5:c.2664C>T MANE Select	NP_004027.2:p.Asn888=