Canonical Allele Identifier: CA346063632

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047321T>A (hg19) ; chr2:g.24824452T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824452T>A , CM000664.2:g.24824452T>A	GRCh38
NC_000002.11:g.25047321T>A , CM000664.1:g.25047321T>A	GRCh37
NC_000002.10:g.24900825T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2665A>T	ENSP00000384484.2:p.Asn889Tyr
ENST00000679454.1:c.2662A>T MANE Select	ENSP00000505261.1:p.Asn888Tyr
ENST00000260600.9:c.2662A>T	ENSP00000260600.5:p.Asn888Tyr
ENST00000405392.5:c.2665A>T	ENSP00000384484.2:p.Asn889Tyr
ENST00000606682.5:c.1603A>T	ENSP00000475652.1:p.Asn535Tyr
NM_004036.3:c.2662A>T	NP_004027.2:p.Asn888Tyr
XM_005264104.1:c.2665A>T	XP_005264161.1:p.Asn889Tyr
XM_005264105.1:c.2662A>T	XP_005264162.1:p.Asn888Tyr
XM_006711925.1:c.2731A>T	XP_006711988.1:p.Asn911Tyr
XM_011532489.1:c.2788A>T	XP_011530791.1:p.Asn930Tyr
XM_011532490.1:c.2785A>T	XP_011530792.1:p.Asn929Tyr
XM_011532491.1:c.2722A>T	XP_011530793.1:p.Asn908Tyr
XM_011532492.1:c.2788A>T	XP_011530794.1:p.Asn930Tyr
XM_011532493.1:c.2650A>T	XP_011530795.1:p.Asn884Tyr
XM_011532494.1:c.2590A>T	XP_011530796.1:p.Asn864Tyr
XM_011532495.1:c.2122A>T	XP_011530797.1:p.Asn708Tyr
XM_011532496.1:c.2065A>T	XP_011530798.1:p.Asn689Tyr
NM_001320613.1:c.2665A>T	NP_001307542.1:p.Asn889Tyr
NM_004036.4:c.2662A>T	NP_004027.2:p.Asn888Tyr
XM_011532492.2:c.2788A>T	XP_011530794.1:p.Asn930Tyr
XM_017003186.1:c.2728A>T	XP_016858675.1:p.Asn910Tyr
XM_017003187.1:c.2719A>T	XP_016858676.1:p.Asn907Tyr
XM_017003188.1:c.2785A>T	XP_016858677.1:p.Asn929Tyr
XM_017003189.1:c.2647A>T	XP_016858678.1:p.Asn883Tyr
XM_017003190.1:c.2524A>T	XP_016858679.1:p.Asn842Tyr
XM_017003191.1:c.2152A>T	XP_016858680.1:p.Asn718Tyr
XM_017003192.1:c.1942A>T	XP_016858681.1:p.Asn648Tyr
XM_017003193.1:c.1939A>T	XP_016858682.1:p.Asn647Tyr
NM_001320613.2:c.2665A>T	NP_001307542.1:p.Asn889Tyr
NM_001377128.1:c.2728A>T	NP_001364057.1:p.Asn910Tyr
NM_001377129.1:c.2524A>T	NP_001364058.1:p.Asn842Tyr
NM_001377130.1:c.2257A>T	NP_001364059.1:p.Asn753Tyr
NM_001377131.1:c.1939A>T	NP_001364060.1:p.Asn647Tyr
NM_001377132.1:c.2662A>T	NP_001364061.1:p.Asn888Tyr
NM_004036.5:c.2662A>T MANE Select	NP_004027.2:p.Asn888Tyr