Canonical Allele Identifier: CA346063430

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047272A>G (hg19) ; chr2:g.24824403A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824403A>G , CM000664.2:g.24824403A>G	GRCh38
NC_000002.11:g.25047272A>G , CM000664.1:g.25047272A>G	GRCh37
NC_000002.10:g.24900776A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2714T>C	ENSP00000384484.2:p.Phe905Ser
ENST00000679454.1:c.2711T>C MANE Select	ENSP00000505261.1:p.Phe904Ser
ENST00000260600.9:c.2711T>C	ENSP00000260600.5:p.Phe904Ser
ENST00000405392.5:c.2714T>C	ENSP00000384484.2:p.Phe905Ser
ENST00000606682.5:c.1652T>C	ENSP00000475652.1:p.Phe551Ser
NM_004036.3:c.2711T>C	NP_004027.2:p.Phe904Ser
XM_005264104.1:c.2714T>C	XP_005264161.1:p.Phe905Ser
XM_005264105.1:c.2711T>C	XP_005264162.1:p.Phe904Ser
XM_006711925.1:c.2780T>C	XP_006711988.1:p.Phe927Ser
XM_011532489.1:c.2837T>C	XP_011530791.1:p.Phe946Ser
XM_011532490.1:c.2834T>C	XP_011530792.1:p.Phe945Ser
XM_011532491.1:c.2771T>C	XP_011530793.1:p.Phe924Ser
XM_011532492.1:c.2837T>C	XP_011530794.1:p.Phe946Ser
XM_011532493.1:c.2699T>C	XP_011530795.1:p.Phe900Ser
XM_011532494.1:c.2639T>C	XP_011530796.1:p.Phe880Ser
XM_011532495.1:c.2171T>C	XP_011530797.1:p.Phe724Ser
XM_011532496.1:c.2114T>C	XP_011530798.1:p.Phe705Ser
NM_001320613.1:c.2714T>C	NP_001307542.1:p.Phe905Ser
NM_004036.4:c.2711T>C	NP_004027.2:p.Phe904Ser
XM_011532492.2:c.2837T>C	XP_011530794.1:p.Phe946Ser
XM_017003186.1:c.2777T>C	XP_016858675.1:p.Phe926Ser
XM_017003187.1:c.2768T>C	XP_016858676.1:p.Phe923Ser
XM_017003188.1:c.2834T>C	XP_016858677.1:p.Phe945Ser
XM_017003189.1:c.2696T>C	XP_016858678.1:p.Phe899Ser
XM_017003190.1:c.2573T>C	XP_016858679.1:p.Phe858Ser
XM_017003191.1:c.2201T>C	XP_016858680.1:p.Phe734Ser
XM_017003192.1:c.1991T>C	XP_016858681.1:p.Phe664Ser
XM_017003193.1:c.1988T>C	XP_016858682.1:p.Phe663Ser
NM_001320613.2:c.2714T>C	NP_001307542.1:p.Phe905Ser
NM_001377128.1:c.2777T>C	NP_001364057.1:p.Phe926Ser
NM_001377129.1:c.2573T>C	NP_001364058.1:p.Phe858Ser
NM_001377130.1:c.2306T>C	NP_001364059.1:p.Phe769Ser
NM_001377131.1:c.1988T>C	NP_001364060.1:p.Phe663Ser
NM_001377132.1:c.2711T>C	NP_001364061.1:p.Phe904Ser
NM_004036.5:c.2711T>C MANE Select	NP_004027.2:p.Phe904Ser