Canonical Allele Identifier: CA425171955

Gene: ADCY3

Linked Data

• gnomAD v4: 2-24823239-G-A
• MyVariant Identifiers: chr2:g.25046108G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823239G>A , CM000664.2:g.24823239G>A	GRCh38
NC_000002.11:g.25046108G>A , CM000664.1:g.25046108G>A	GRCh37
NC_000002.10:g.24899612G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2856C>T	ENSP00000384484.2:p.Phe952=
ENST00000679454.1:c.2853C>T MANE Select	ENSP00000505261.1:p.Phe951=
ENST00000260600.9:c.2853C>T	ENSP00000260600.5:p.Phe951=
ENST00000405392.5:c.2856C>T	ENSP00000384484.2:p.Phe952=
ENST00000485887.1:n.125C>T
ENST00000606682.5:c.1794C>T	ENSP00000475652.1:p.Phe598=
NM_004036.3:c.2853C>T	NP_004027.2:p.Phe951=
XM_005264104.1:c.2856C>T	XP_005264161.1:p.Phe952=
XM_005264105.1:c.2853C>T	XP_005264162.1:p.Phe951=
XM_006711925.1:c.2922C>T	XP_006711988.1:p.Phe974=
XM_011532489.1:c.2979C>T	XP_011530791.1:p.Phe993=
XM_011532490.1:c.2976C>T	XP_011530792.1:p.Phe992=
XM_011532491.1:c.2913C>T	XP_011530793.1:p.Phe971=
XM_011532492.1:c.2979C>T	XP_011530794.1:p.Phe993=
XM_011532493.1:c.2841C>T	XP_011530795.1:p.Phe947=
XM_011532494.1:c.2781C>T	XP_011530796.1:p.Phe927=
XM_011532495.1:c.2313C>T	XP_011530797.1:p.Phe771=
XM_011532496.1:c.2256C>T	XP_011530798.1:p.Phe752=
NM_001320613.1:c.2856C>T	NP_001307542.1:p.Phe952=
NM_004036.4:c.2853C>T	NP_004027.2:p.Phe951=
XM_011532492.2:c.2979C>T	XP_011530794.1:p.Phe993=
XM_017003186.1:c.2919C>T	XP_016858675.1:p.Phe973=
XM_017003187.1:c.2910C>T	XP_016858676.1:p.Phe970=
XM_017003188.1:c.2976C>T	XP_016858677.1:p.Phe992=
XM_017003189.1:c.2838C>T	XP_016858678.1:p.Phe946=
XM_017003190.1:c.2715C>T	XP_016858679.1:p.Phe905=
XM_017003191.1:c.2343C>T	XP_016858680.1:p.Phe781=
XM_017003192.1:c.2133C>T	XP_016858681.1:p.Phe711=
XM_017003193.1:c.2130C>T	XP_016858682.1:p.Phe710=
NM_001320613.2:c.2856C>T	NP_001307542.1:p.Phe952=
NM_001377128.1:c.2919C>T	NP_001364057.1:p.Phe973=
NM_001377129.1:c.2715C>T	NP_001364058.1:p.Phe905=
NM_001377130.1:c.2332-609C>T	NP_001364059.1:n.2332-609C>T
NM_001377131.1:c.2130C>T	NP_001364060.1:p.Phe710=
NM_001377132.1:c.2853C>T	NP_001364061.1:p.Phe951=
NM_004036.5:c.2853C>T MANE Select	NP_004027.2:p.Phe951=