Canonical Allele Identifier: CA346063627

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047320T>A (hg19) ; chr2:g.24824451T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824451T>A , CM000664.2:g.24824451T>A	GRCh38
NC_000002.11:g.25047320T>A , CM000664.1:g.25047320T>A	GRCh37
NC_000002.10:g.24900824T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2666A>T	ENSP00000384484.2:p.Asn889Ile
ENST00000679454.1:c.2663A>T MANE Select	ENSP00000505261.1:p.Asn888Ile
ENST00000260600.9:c.2663A>T	ENSP00000260600.5:p.Asn888Ile
ENST00000405392.5:c.2666A>T	ENSP00000384484.2:p.Asn889Ile
ENST00000606682.5:c.1604A>T	ENSP00000475652.1:p.Asn535Ile
NM_004036.3:c.2663A>T	NP_004027.2:p.Asn888Ile
XM_005264104.1:c.2666A>T	XP_005264161.1:p.Asn889Ile
XM_005264105.1:c.2663A>T	XP_005264162.1:p.Asn888Ile
XM_006711925.1:c.2732A>T	XP_006711988.1:p.Asn911Ile
XM_011532489.1:c.2789A>T	XP_011530791.1:p.Asn930Ile
XM_011532490.1:c.2786A>T	XP_011530792.1:p.Asn929Ile
XM_011532491.1:c.2723A>T	XP_011530793.1:p.Asn908Ile
XM_011532492.1:c.2789A>T	XP_011530794.1:p.Asn930Ile
XM_011532493.1:c.2651A>T	XP_011530795.1:p.Asn884Ile
XM_011532494.1:c.2591A>T	XP_011530796.1:p.Asn864Ile
XM_011532495.1:c.2123A>T	XP_011530797.1:p.Asn708Ile
XM_011532496.1:c.2066A>T	XP_011530798.1:p.Asn689Ile
NM_001320613.1:c.2666A>T	NP_001307542.1:p.Asn889Ile
NM_004036.4:c.2663A>T	NP_004027.2:p.Asn888Ile
XM_011532492.2:c.2789A>T	XP_011530794.1:p.Asn930Ile
XM_017003186.1:c.2729A>T	XP_016858675.1:p.Asn910Ile
XM_017003187.1:c.2720A>T	XP_016858676.1:p.Asn907Ile
XM_017003188.1:c.2786A>T	XP_016858677.1:p.Asn929Ile
XM_017003189.1:c.2648A>T	XP_016858678.1:p.Asn883Ile
XM_017003190.1:c.2525A>T	XP_016858679.1:p.Asn842Ile
XM_017003191.1:c.2153A>T	XP_016858680.1:p.Asn718Ile
XM_017003192.1:c.1943A>T	XP_016858681.1:p.Asn648Ile
XM_017003193.1:c.1940A>T	XP_016858682.1:p.Asn647Ile
NM_001320613.2:c.2666A>T	NP_001307542.1:p.Asn889Ile
NM_001377128.1:c.2729A>T	NP_001364057.1:p.Asn910Ile
NM_001377129.1:c.2525A>T	NP_001364058.1:p.Asn842Ile
NM_001377130.1:c.2258A>T	NP_001364059.1:p.Asn753Ile
NM_001377131.1:c.1940A>T	NP_001364060.1:p.Asn647Ile
NM_001377132.1:c.2663A>T	NP_001364061.1:p.Asn888Ile
NM_004036.5:c.2663A>T MANE Select	NP_004027.2:p.Asn888Ile