Canonical Allele Identifier: CA346063594

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047309C>A (hg19) ; chr2:g.24824440C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824440C>A , CM000664.2:g.24824440C>A	GRCh38
NC_000002.11:g.25047309C>A , CM000664.1:g.25047309C>A	GRCh37
NC_000002.10:g.24900813C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2677G>T	ENSP00000384484.2:p.Val893Phe
ENST00000679454.1:c.2674G>T MANE Select	ENSP00000505261.1:p.Val892Phe
ENST00000260600.9:c.2674G>T	ENSP00000260600.5:p.Val892Phe
ENST00000405392.5:c.2677G>T	ENSP00000384484.2:p.Val893Phe
ENST00000606682.5:c.1615G>T	ENSP00000475652.1:p.Val539Phe
NM_004036.3:c.2674G>T	NP_004027.2:p.Val892Phe
XM_005264104.1:c.2677G>T	XP_005264161.1:p.Val893Phe
XM_005264105.1:c.2674G>T	XP_005264162.1:p.Val892Phe
XM_006711925.1:c.2743G>T	XP_006711988.1:p.Val915Phe
XM_011532489.1:c.2800G>T	XP_011530791.1:p.Val934Phe
XM_011532490.1:c.2797G>T	XP_011530792.1:p.Val933Phe
XM_011532491.1:c.2734G>T	XP_011530793.1:p.Val912Phe
XM_011532492.1:c.2800G>T	XP_011530794.1:p.Val934Phe
XM_011532493.1:c.2662G>T	XP_011530795.1:p.Val888Phe
XM_011532494.1:c.2602G>T	XP_011530796.1:p.Val868Phe
XM_011532495.1:c.2134G>T	XP_011530797.1:p.Val712Phe
XM_011532496.1:c.2077G>T	XP_011530798.1:p.Val693Phe
NM_001320613.1:c.2677G>T	NP_001307542.1:p.Val893Phe
NM_004036.4:c.2674G>T	NP_004027.2:p.Val892Phe
XM_011532492.2:c.2800G>T	XP_011530794.1:p.Val934Phe
XM_017003186.1:c.2740G>T	XP_016858675.1:p.Val914Phe
XM_017003187.1:c.2731G>T	XP_016858676.1:p.Val911Phe
XM_017003188.1:c.2797G>T	XP_016858677.1:p.Val933Phe
XM_017003189.1:c.2659G>T	XP_016858678.1:p.Val887Phe
XM_017003190.1:c.2536G>T	XP_016858679.1:p.Val846Phe
XM_017003191.1:c.2164G>T	XP_016858680.1:p.Val722Phe
XM_017003192.1:c.1954G>T	XP_016858681.1:p.Val652Phe
XM_017003193.1:c.1951G>T	XP_016858682.1:p.Val651Phe
NM_001320613.2:c.2677G>T	NP_001307542.1:p.Val893Phe
NM_001377128.1:c.2740G>T	NP_001364057.1:p.Val914Phe
NM_001377129.1:c.2536G>T	NP_001364058.1:p.Val846Phe
NM_001377130.1:c.2269G>T	NP_001364059.1:p.Val757Phe
NM_001377131.1:c.1951G>T	NP_001364060.1:p.Val651Phe
NM_001377132.1:c.2674G>T	NP_001364061.1:p.Val892Phe
NM_004036.5:c.2674G>T MANE Select	NP_004027.2:p.Val892Phe