Canonical Allele Identifier: CA346063609

Gene: ADCY3

Linked Data

• dbSNP Id: rs1438206069
• MyVariant Identifiers: chr2:g.25047314G>A (hg19) ; chr2:g.24824445G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824445G>A , CM000664.2:g.24824445G>A	GRCh38
NC_000002.11:g.25047314G>A , CM000664.1:g.25047314G>A	GRCh37
NC_000002.10:g.24900818G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2672C>T	ENSP00000384484.2:p.Ala891Val
ENST00000679454.1:c.2669C>T MANE Select	ENSP00000505261.1:p.Ala890Val
ENST00000260600.9:c.2669C>T	ENSP00000260600.5:p.Ala890Val
ENST00000405392.5:c.2672C>T	ENSP00000384484.2:p.Ala891Val
ENST00000606682.5:c.1610C>T	ENSP00000475652.1:p.Ala537Val
NM_004036.3:c.2669C>T	NP_004027.2:p.Ala890Val
XM_005264104.1:c.2672C>T	XP_005264161.1:p.Ala891Val
XM_005264105.1:c.2669C>T	XP_005264162.1:p.Ala890Val
XM_006711925.1:c.2738C>T	XP_006711988.1:p.Ala913Val
XM_011532489.1:c.2795C>T	XP_011530791.1:p.Ala932Val
XM_011532490.1:c.2792C>T	XP_011530792.1:p.Ala931Val
XM_011532491.1:c.2729C>T	XP_011530793.1:p.Ala910Val
XM_011532492.1:c.2795C>T	XP_011530794.1:p.Ala932Val
XM_011532493.1:c.2657C>T	XP_011530795.1:p.Ala886Val
XM_011532494.1:c.2597C>T	XP_011530796.1:p.Ala866Val
XM_011532495.1:c.2129C>T	XP_011530797.1:p.Ala710Val
XM_011532496.1:c.2072C>T	XP_011530798.1:p.Ala691Val
NM_001320613.1:c.2672C>T	NP_001307542.1:p.Ala891Val
NM_004036.4:c.2669C>T	NP_004027.2:p.Ala890Val
XM_011532492.2:c.2795C>T	XP_011530794.1:p.Ala932Val
XM_017003186.1:c.2735C>T	XP_016858675.1:p.Ala912Val
XM_017003187.1:c.2726C>T	XP_016858676.1:p.Ala909Val
XM_017003188.1:c.2792C>T	XP_016858677.1:p.Ala931Val
XM_017003189.1:c.2654C>T	XP_016858678.1:p.Ala885Val
XM_017003190.1:c.2531C>T	XP_016858679.1:p.Ala844Val
XM_017003191.1:c.2159C>T	XP_016858680.1:p.Ala720Val
XM_017003192.1:c.1949C>T	XP_016858681.1:p.Ala650Val
XM_017003193.1:c.1946C>T	XP_016858682.1:p.Ala649Val
NM_001320613.2:c.2672C>T	NP_001307542.1:p.Ala891Val
NM_001377128.1:c.2735C>T	NP_001364057.1:p.Ala912Val
NM_001377129.1:c.2531C>T	NP_001364058.1:p.Ala844Val
NM_001377130.1:c.2264C>T	NP_001364059.1:p.Ala755Val
NM_001377131.1:c.1946C>T	NP_001364060.1:p.Ala649Val
NM_001377132.1:c.2669C>T	NP_001364061.1:p.Ala890Val
NM_004036.5:c.2669C>T MANE Select	NP_004027.2:p.Ala890Val