Canonical Allele Identifier: CA346063642

Gene: ADCY3

Linked Data

• gnomAD v4: 2-24824454-C-T
• MyVariant Identifiers: chr2:g.25047323C>T (hg19) ; chr2:g.24824454C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2663G>A	ENSP00000384484.2:p.Trp888Ter
ENST00000679454.1:c.2660G>A MANE Select	ENSP00000505261.1:p.Trp887Ter
ENST00000260600.9:c.2660G>A	ENSP00000260600.5:p.Trp887Ter
ENST00000405392.5:c.2663G>A	ENSP00000384484.2:p.Trp888Ter
ENST00000606682.5:c.1601G>A	ENSP00000475652.1:p.Trp534Ter
NM_004036.3:c.2660G>A	NP_004027.2:p.Trp887Ter
XM_005264104.1:c.2663G>A	XP_005264161.1:p.Trp888Ter
XM_005264105.1:c.2660G>A	XP_005264162.1:p.Trp887Ter
XM_006711925.1:c.2729G>A	XP_006711988.1:p.Trp910Ter
XM_011532489.1:c.2786G>A	XP_011530791.1:p.Trp929Ter
XM_011532490.1:c.2783G>A	XP_011530792.1:p.Trp928Ter
XM_011532491.1:c.2720G>A	XP_011530793.1:p.Trp907Ter
XM_011532492.1:c.2786G>A	XP_011530794.1:p.Trp929Ter
XM_011532493.1:c.2648G>A	XP_011530795.1:p.Trp883Ter
XM_011532494.1:c.2588G>A	XP_011530796.1:p.Trp863Ter
XM_011532495.1:c.2120G>A	XP_011530797.1:p.Trp707Ter
XM_011532496.1:c.2063G>A	XP_011530798.1:p.Trp688Ter
NM_001320613.1:c.2663G>A	NP_001307542.1:p.Trp888Ter
NM_004036.4:c.2660G>A	NP_004027.2:p.Trp887Ter
XM_011532492.2:c.2786G>A	XP_011530794.1:p.Trp929Ter
XM_017003186.1:c.2726G>A	XP_016858675.1:p.Trp909Ter
XM_017003187.1:c.2717G>A	XP_016858676.1:p.Trp906Ter
XM_017003188.1:c.2783G>A	XP_016858677.1:p.Trp928Ter
XM_017003189.1:c.2645G>A	XP_016858678.1:p.Trp882Ter
XM_017003190.1:c.2522G>A	XP_016858679.1:p.Trp841Ter
XM_017003191.1:c.2150G>A	XP_016858680.1:p.Trp717Ter
XM_017003192.1:c.1940G>A	XP_016858681.1:p.Trp647Ter
XM_017003193.1:c.1937G>A	XP_016858682.1:p.Trp646Ter
NM_001320613.2:c.2663G>A	NP_001307542.1:p.Trp888Ter
NM_001377128.1:c.2726G>A	NP_001364057.1:p.Trp909Ter
NM_001377129.1:c.2522G>A	NP_001364058.1:p.Trp841Ter
NM_001377130.1:c.2255G>A	NP_001364059.1:p.Trp752Ter
NM_001377131.1:c.1937G>A	NP_001364060.1:p.Trp646Ter
NM_001377132.1:c.2660G>A	NP_001364061.1:p.Trp887Ter
NM_004036.5:c.2660G>A MANE Select	NP_004027.2:p.Trp887Ter