Canonical Allele Identifier: CA346063629

Gene: ADCY3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2666A>C	ENSP00000384484.2:p.Asn889Thr
ENST00000679454.1:c.2663A>C MANE Select	ENSP00000505261.1:p.Asn888Thr
ENST00000260600.9:c.2663A>C	ENSP00000260600.5:p.Asn888Thr
ENST00000405392.5:c.2666A>C	ENSP00000384484.2:p.Asn889Thr
ENST00000606682.5:c.1604A>C	ENSP00000475652.1:p.Asn535Thr
NM_004036.3:c.2663A>C	NP_004027.2:p.Asn888Thr
XM_005264104.1:c.2666A>C	XP_005264161.1:p.Asn889Thr
XM_005264105.1:c.2663A>C	XP_005264162.1:p.Asn888Thr
XM_006711925.1:c.2732A>C	XP_006711988.1:p.Asn911Thr
XM_011532489.1:c.2789A>C	XP_011530791.1:p.Asn930Thr
XM_011532490.1:c.2786A>C	XP_011530792.1:p.Asn929Thr
XM_011532491.1:c.2723A>C	XP_011530793.1:p.Asn908Thr
XM_011532492.1:c.2789A>C	XP_011530794.1:p.Asn930Thr
XM_011532493.1:c.2651A>C	XP_011530795.1:p.Asn884Thr
XM_011532494.1:c.2591A>C	XP_011530796.1:p.Asn864Thr
XM_011532495.1:c.2123A>C	XP_011530797.1:p.Asn708Thr
XM_011532496.1:c.2066A>C	XP_011530798.1:p.Asn689Thr
NM_001320613.1:c.2666A>C	NP_001307542.1:p.Asn889Thr
NM_004036.4:c.2663A>C	NP_004027.2:p.Asn888Thr
XM_011532492.2:c.2789A>C	XP_011530794.1:p.Asn930Thr
XM_017003186.1:c.2729A>C	XP_016858675.1:p.Asn910Thr
XM_017003187.1:c.2720A>C	XP_016858676.1:p.Asn907Thr
XM_017003188.1:c.2786A>C	XP_016858677.1:p.Asn929Thr
XM_017003189.1:c.2648A>C	XP_016858678.1:p.Asn883Thr
XM_017003190.1:c.2525A>C	XP_016858679.1:p.Asn842Thr
XM_017003191.1:c.2153A>C	XP_016858680.1:p.Asn718Thr
XM_017003192.1:c.1943A>C	XP_016858681.1:p.Asn648Thr
XM_017003193.1:c.1940A>C	XP_016858682.1:p.Asn647Thr
NM_001320613.2:c.2666A>C	NP_001307542.1:p.Asn889Thr
NM_001377128.1:c.2729A>C	NP_001364057.1:p.Asn910Thr
NM_001377129.1:c.2525A>C	NP_001364058.1:p.Asn842Thr
NM_001377130.1:c.2258A>C	NP_001364059.1:p.Asn753Thr
NM_001377131.1:c.1940A>C	NP_001364060.1:p.Asn647Thr
NM_001377132.1:c.2663A>C	NP_001364061.1:p.Asn888Thr
NM_004036.5:c.2663A>C MANE Select	NP_004027.2:p.Asn888Thr