Canonical Allele Identifier: CA346063701

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047341A>C (hg19) ; chr2:g.24824472A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824472A>C , CM000664.2:g.24824472A>C	GRCh38
NC_000002.11:g.25047341A>C , CM000664.1:g.25047341A>C	GRCh37
NC_000002.10:g.24900845A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2645T>G	ENSP00000384484.2:p.Val882Gly
ENST00000679454.1:c.2642T>G MANE Select	ENSP00000505261.1:p.Val881Gly
ENST00000260600.9:c.2642T>G	ENSP00000260600.5:p.Val881Gly
ENST00000405392.5:c.2645T>G	ENSP00000384484.2:p.Val882Gly
ENST00000606682.5:c.1583T>G	ENSP00000475652.1:p.Val528Gly
NM_004036.3:c.2642T>G	NP_004027.2:p.Val881Gly
XM_005264104.1:c.2645T>G	XP_005264161.1:p.Val882Gly
XM_005264105.1:c.2642T>G	XP_005264162.1:p.Val881Gly
XM_006711925.1:c.2711T>G	XP_006711988.1:p.Val904Gly
XM_011532489.1:c.2768T>G	XP_011530791.1:p.Val923Gly
XM_011532490.1:c.2765T>G	XP_011530792.1:p.Val922Gly
XM_011532491.1:c.2702T>G	XP_011530793.1:p.Val901Gly
XM_011532492.1:c.2768T>G	XP_011530794.1:p.Val923Gly
XM_011532493.1:c.2630T>G	XP_011530795.1:p.Val877Gly
XM_011532494.1:c.2570T>G	XP_011530796.1:p.Val857Gly
XM_011532495.1:c.2102T>G	XP_011530797.1:p.Val701Gly
XM_011532496.1:c.2045T>G	XP_011530798.1:p.Val682Gly
NM_001320613.1:c.2645T>G	NP_001307542.1:p.Val882Gly
NM_004036.4:c.2642T>G	NP_004027.2:p.Val881Gly
XM_011532492.2:c.2768T>G	XP_011530794.1:p.Val923Gly
XM_017003186.1:c.2708T>G	XP_016858675.1:p.Val903Gly
XM_017003187.1:c.2699T>G	XP_016858676.1:p.Val900Gly
XM_017003188.1:c.2765T>G	XP_016858677.1:p.Val922Gly
XM_017003189.1:c.2627T>G	XP_016858678.1:p.Val876Gly
XM_017003190.1:c.2504T>G	XP_016858679.1:p.Val835Gly
XM_017003191.1:c.2132T>G	XP_016858680.1:p.Val711Gly
XM_017003192.1:c.1922T>G	XP_016858681.1:p.Val641Gly
XM_017003193.1:c.1919T>G	XP_016858682.1:p.Val640Gly
NM_001320613.2:c.2645T>G	NP_001307542.1:p.Val882Gly
NM_001377128.1:c.2708T>G	NP_001364057.1:p.Val903Gly
NM_001377129.1:c.2504T>G	NP_001364058.1:p.Val835Gly
NM_001377130.1:c.2237T>G	NP_001364059.1:p.Val746Gly
NM_001377131.1:c.1919T>G	NP_001364060.1:p.Val640Gly
NM_001377132.1:c.2642T>G	NP_001364061.1:p.Val881Gly
NM_004036.5:c.2642T>G MANE Select	NP_004027.2:p.Val881Gly