Canonical Allele Identifier: CA346063636

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047322C>T (hg19) ; chr2:g.24824453C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824453C>T , CM000664.2:g.24824453C>T	GRCh38
NC_000002.11:g.25047322C>T , CM000664.1:g.25047322C>T	GRCh37
NC_000002.10:g.24900826C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2664G>A	ENSP00000384484.2:p.Trp888Ter
ENST00000679454.1:c.2661G>A MANE Select	ENSP00000505261.1:p.Trp887Ter
ENST00000260600.9:c.2661G>A	ENSP00000260600.5:p.Trp887Ter
ENST00000405392.5:c.2664G>A	ENSP00000384484.2:p.Trp888Ter
ENST00000606682.5:c.1602G>A	ENSP00000475652.1:p.Trp534Ter
NM_004036.3:c.2661G>A	NP_004027.2:p.Trp887Ter
XM_005264104.1:c.2664G>A	XP_005264161.1:p.Trp888Ter
XM_005264105.1:c.2661G>A	XP_005264162.1:p.Trp887Ter
XM_006711925.1:c.2730G>A	XP_006711988.1:p.Trp910Ter
XM_011532489.1:c.2787G>A	XP_011530791.1:p.Trp929Ter
XM_011532490.1:c.2784G>A	XP_011530792.1:p.Trp928Ter
XM_011532491.1:c.2721G>A	XP_011530793.1:p.Trp907Ter
XM_011532492.1:c.2787G>A	XP_011530794.1:p.Trp929Ter
XM_011532493.1:c.2649G>A	XP_011530795.1:p.Trp883Ter
XM_011532494.1:c.2589G>A	XP_011530796.1:p.Trp863Ter
XM_011532495.1:c.2121G>A	XP_011530797.1:p.Trp707Ter
XM_011532496.1:c.2064G>A	XP_011530798.1:p.Trp688Ter
NM_001320613.1:c.2664G>A	NP_001307542.1:p.Trp888Ter
NM_004036.4:c.2661G>A	NP_004027.2:p.Trp887Ter
XM_011532492.2:c.2787G>A	XP_011530794.1:p.Trp929Ter
XM_017003186.1:c.2727G>A	XP_016858675.1:p.Trp909Ter
XM_017003187.1:c.2718G>A	XP_016858676.1:p.Trp906Ter
XM_017003188.1:c.2784G>A	XP_016858677.1:p.Trp928Ter
XM_017003189.1:c.2646G>A	XP_016858678.1:p.Trp882Ter
XM_017003190.1:c.2523G>A	XP_016858679.1:p.Trp841Ter
XM_017003191.1:c.2151G>A	XP_016858680.1:p.Trp717Ter
XM_017003192.1:c.1941G>A	XP_016858681.1:p.Trp647Ter
XM_017003193.1:c.1938G>A	XP_016858682.1:p.Trp646Ter
NM_001320613.2:c.2664G>A	NP_001307542.1:p.Trp888Ter
NM_001377128.1:c.2727G>A	NP_001364057.1:p.Trp909Ter
NM_001377129.1:c.2523G>A	NP_001364058.1:p.Trp841Ter
NM_001377130.1:c.2256G>A	NP_001364059.1:p.Trp752Ter
NM_001377131.1:c.1938G>A	NP_001364060.1:p.Trp646Ter
NM_001377132.1:c.2661G>A	NP_001364061.1:p.Trp887Ter
NM_004036.5:c.2661G>A MANE Select	NP_004027.2:p.Trp887Ter