Canonical Allele Identifier: CA346062877

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046167A>G (hg19) ; chr2:g.24823298A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823298A>G , CM000664.2:g.24823298A>G	GRCh38
NC_000002.11:g.25046167A>G , CM000664.1:g.25046167A>G	GRCh37
NC_000002.10:g.24899671A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2797T>C	ENSP00000384484.2:p.Phe933Leu
ENST00000679454.1:c.2794T>C MANE Select	ENSP00000505261.1:p.Phe932Leu
ENST00000260600.9:c.2794T>C	ENSP00000260600.5:p.Phe932Leu
ENST00000405392.5:c.2797T>C	ENSP00000384484.2:p.Phe933Leu
ENST00000485887.1:n.66T>C
ENST00000606682.5:c.1735T>C	ENSP00000475652.1:p.Phe579Leu
NM_004036.3:c.2794T>C	NP_004027.2:p.Phe932Leu
XM_005264104.1:c.2797T>C	XP_005264161.1:p.Phe933Leu
XM_005264105.1:c.2794T>C	XP_005264162.1:p.Phe932Leu
XM_006711925.1:c.2863T>C	XP_006711988.1:p.Phe955Leu
XM_011532489.1:c.2920T>C	XP_011530791.1:p.Phe974Leu
XM_011532490.1:c.2917T>C	XP_011530792.1:p.Phe973Leu
XM_011532491.1:c.2854T>C	XP_011530793.1:p.Phe952Leu
XM_011532492.1:c.2920T>C	XP_011530794.1:p.Phe974Leu
XM_011532493.1:c.2782T>C	XP_011530795.1:p.Phe928Leu
XM_011532494.1:c.2722T>C	XP_011530796.1:p.Phe908Leu
XM_011532495.1:c.2254T>C	XP_011530797.1:p.Phe752Leu
XM_011532496.1:c.2197T>C	XP_011530798.1:p.Phe733Leu
NM_001320613.1:c.2797T>C	NP_001307542.1:p.Phe933Leu
NM_004036.4:c.2794T>C	NP_004027.2:p.Phe932Leu
XM_011532492.2:c.2920T>C	XP_011530794.1:p.Phe974Leu
XM_017003186.1:c.2860T>C	XP_016858675.1:p.Phe954Leu
XM_017003187.1:c.2851T>C	XP_016858676.1:p.Phe951Leu
XM_017003188.1:c.2917T>C	XP_016858677.1:p.Phe973Leu
XM_017003189.1:c.2779T>C	XP_016858678.1:p.Phe927Leu
XM_017003190.1:c.2656T>C	XP_016858679.1:p.Phe886Leu
XM_017003191.1:c.2284T>C	XP_016858680.1:p.Phe762Leu
XM_017003192.1:c.2074T>C	XP_016858681.1:p.Phe692Leu
XM_017003193.1:c.2071T>C	XP_016858682.1:p.Phe691Leu
NM_001320613.2:c.2797T>C	NP_001307542.1:p.Phe933Leu
NM_001377128.1:c.2860T>C	NP_001364057.1:p.Phe954Leu
NM_001377129.1:c.2656T>C	NP_001364058.1:p.Phe886Leu
NM_001377130.1:c.2332-668T>C	NP_001364059.1:n.2332-668T>C
NM_001377131.1:c.2071T>C	NP_001364060.1:p.Phe691Leu
NM_001377132.1:c.2794T>C	NP_001364061.1:p.Phe932Leu
NM_004036.5:c.2794T>C MANE Select	NP_004027.2:p.Phe932Leu