Canonical Allele Identifier: CA1553562

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24822532A>G , CM000664.2:g.24822532A>G	GRCh38
NC_000002.11:g.25045401A>G , CM000664.1:g.25045401A>G	GRCh37
NC_000002.10:g.24898905A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2985T>C	ENSP00000384484.2:p.Asn995=
ENST00000679454.1:c.2982T>C MANE Select	ENSP00000505261.1:p.Asn994=
ENST00000260600.9:c.2982T>C	ENSP00000260600.5:p.Asn994=
ENST00000405392.5:c.2985T>C	ENSP00000384484.2:p.Asn995=
ENST00000485887.1:n.254T>C
ENST00000606682.5:c.1923T>C	ENSP00000475652.1:p.Asn641=
NM_004036.3:c.2982T>C	NP_004027.2:p.Asn994=
XM_005264104.1:c.2985T>C	XP_005264161.1:p.Asn995=
XM_005264105.1:c.2982T>C	XP_005264162.1:p.Asn994=
XM_006711925.1:c.3051T>C	XP_006711988.1:p.Asn1017=
XM_011532489.1:c.3108T>C	XP_011530791.1:p.Asn1036=
XM_011532490.1:c.3105T>C	XP_011530792.1:p.Asn1035=
XM_011532491.1:c.3042T>C	XP_011530793.1:p.Asn1014=
XM_011532492.1:c.3108T>C	XP_011530794.1:p.Asn1036=
XM_011532493.1:c.2970T>C	XP_011530795.1:p.Asn990=
XM_011532494.1:c.2910T>C	XP_011530796.1:p.Asn970=
XM_011532495.1:c.2442T>C	XP_011530797.1:p.Asn814=
XM_011532496.1:c.2385T>C	XP_011530798.1:p.Asn795=
NM_001320613.1:c.2985T>C	NP_001307542.1:p.Asn995=
NM_004036.4:c.2982T>C	NP_004027.2:p.Asn994=
XM_011532492.2:c.3108T>C	XP_011530794.1:p.Asn1036=
XM_017003186.1:c.3048T>C	XP_016858675.1:p.Asn1016=
XM_017003187.1:c.3039T>C	XP_016858676.1:p.Asn1013=
XM_017003188.1:c.3105T>C	XP_016858677.1:p.Asn1035=
XM_017003189.1:c.2967T>C	XP_016858678.1:p.Asn989=
XM_017003190.1:c.2844T>C	XP_016858679.1:p.Asn948=
XM_017003191.1:c.2472T>C	XP_016858680.1:p.Asn824=
XM_017003192.1:c.2262T>C	XP_016858681.1:p.Asn754=
XM_017003193.1:c.2259T>C	XP_016858682.1:p.Asn753=
NM_001320613.2:c.2985T>C	NP_001307542.1:p.Asn995=
NM_001377128.1:c.3048T>C	NP_001364057.1:p.Asn1016=
NM_001377129.1:c.2844T>C	NP_001364058.1:p.Asn948=
NM_001377130.1:c.2430T>C	NP_001364059.1:p.Asn810=
NM_001377131.1:c.2259T>C	NP_001364060.1:p.Asn753=
NM_001377132.1:c.2982T>C	NP_001364061.1:p.Asn994=
NM_004036.5:c.2982T>C MANE Select	NP_004027.2:p.Asn994=