Canonical Allele Identifier: CA346063639

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047323C>A (hg19) ; chr2:g.24824454C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824454C>A , CM000664.2:g.24824454C>A	GRCh38
NC_000002.11:g.25047323C>A , CM000664.1:g.25047323C>A	GRCh37
NC_000002.10:g.24900827C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2663G>T	ENSP00000384484.2:p.Trp888Leu
ENST00000679454.1:c.2660G>T MANE Select	ENSP00000505261.1:p.Trp887Leu
ENST00000260600.9:c.2660G>T	ENSP00000260600.5:p.Trp887Leu
ENST00000405392.5:c.2663G>T	ENSP00000384484.2:p.Trp888Leu
ENST00000606682.5:c.1601G>T	ENSP00000475652.1:p.Trp534Leu
NM_004036.3:c.2660G>T	NP_004027.2:p.Trp887Leu
XM_005264104.1:c.2663G>T	XP_005264161.1:p.Trp888Leu
XM_005264105.1:c.2660G>T	XP_005264162.1:p.Trp887Leu
XM_006711925.1:c.2729G>T	XP_006711988.1:p.Trp910Leu
XM_011532489.1:c.2786G>T	XP_011530791.1:p.Trp929Leu
XM_011532490.1:c.2783G>T	XP_011530792.1:p.Trp928Leu
XM_011532491.1:c.2720G>T	XP_011530793.1:p.Trp907Leu
XM_011532492.1:c.2786G>T	XP_011530794.1:p.Trp929Leu
XM_011532493.1:c.2648G>T	XP_011530795.1:p.Trp883Leu
XM_011532494.1:c.2588G>T	XP_011530796.1:p.Trp863Leu
XM_011532495.1:c.2120G>T	XP_011530797.1:p.Trp707Leu
XM_011532496.1:c.2063G>T	XP_011530798.1:p.Trp688Leu
NM_001320613.1:c.2663G>T	NP_001307542.1:p.Trp888Leu
NM_004036.4:c.2660G>T	NP_004027.2:p.Trp887Leu
XM_011532492.2:c.2786G>T	XP_011530794.1:p.Trp929Leu
XM_017003186.1:c.2726G>T	XP_016858675.1:p.Trp909Leu
XM_017003187.1:c.2717G>T	XP_016858676.1:p.Trp906Leu
XM_017003188.1:c.2783G>T	XP_016858677.1:p.Trp928Leu
XM_017003189.1:c.2645G>T	XP_016858678.1:p.Trp882Leu
XM_017003190.1:c.2522G>T	XP_016858679.1:p.Trp841Leu
XM_017003191.1:c.2150G>T	XP_016858680.1:p.Trp717Leu
XM_017003192.1:c.1940G>T	XP_016858681.1:p.Trp647Leu
XM_017003193.1:c.1937G>T	XP_016858682.1:p.Trp646Leu
NM_001320613.2:c.2663G>T	NP_001307542.1:p.Trp888Leu
NM_001377128.1:c.2726G>T	NP_001364057.1:p.Trp909Leu
NM_001377129.1:c.2522G>T	NP_001364058.1:p.Trp841Leu
NM_001377130.1:c.2255G>T	NP_001364059.1:p.Trp752Leu
NM_001377131.1:c.1937G>T	NP_001364060.1:p.Trp646Leu
NM_001377132.1:c.2660G>T	NP_001364061.1:p.Trp887Leu
NM_004036.5:c.2660G>T MANE Select	NP_004027.2:p.Trp887Leu