Canonical Allele Identifier: CA346063673

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047333T>C (hg19) ; chr2:g.24824464T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824464T>C , CM000664.2:g.24824464T>C	GRCh38
NC_000002.11:g.25047333T>C , CM000664.1:g.25047333T>C	GRCh37
NC_000002.10:g.24900837T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2653A>G	ENSP00000384484.2:p.Met885Val
ENST00000679454.1:c.2650A>G MANE Select	ENSP00000505261.1:p.Met884Val
ENST00000260600.9:c.2650A>G	ENSP00000260600.5:p.Met884Val
ENST00000405392.5:c.2653A>G	ENSP00000384484.2:p.Met885Val
ENST00000606682.5:c.1591A>G	ENSP00000475652.1:p.Met531Val
NM_004036.3:c.2650A>G	NP_004027.2:p.Met884Val
XM_005264104.1:c.2653A>G	XP_005264161.1:p.Met885Val
XM_005264105.1:c.2650A>G	XP_005264162.1:p.Met884Val
XM_006711925.1:c.2719A>G	XP_006711988.1:p.Met907Val
XM_011532489.1:c.2776A>G	XP_011530791.1:p.Met926Val
XM_011532490.1:c.2773A>G	XP_011530792.1:p.Met925Val
XM_011532491.1:c.2710A>G	XP_011530793.1:p.Met904Val
XM_011532492.1:c.2776A>G	XP_011530794.1:p.Met926Val
XM_011532493.1:c.2638A>G	XP_011530795.1:p.Met880Val
XM_011532494.1:c.2578A>G	XP_011530796.1:p.Met860Val
XM_011532495.1:c.2110A>G	XP_011530797.1:p.Met704Val
XM_011532496.1:c.2053A>G	XP_011530798.1:p.Met685Val
NM_001320613.1:c.2653A>G	NP_001307542.1:p.Met885Val
NM_004036.4:c.2650A>G	NP_004027.2:p.Met884Val
XM_011532492.2:c.2776A>G	XP_011530794.1:p.Met926Val
XM_017003186.1:c.2716A>G	XP_016858675.1:p.Met906Val
XM_017003187.1:c.2707A>G	XP_016858676.1:p.Met903Val
XM_017003188.1:c.2773A>G	XP_016858677.1:p.Met925Val
XM_017003189.1:c.2635A>G	XP_016858678.1:p.Met879Val
XM_017003190.1:c.2512A>G	XP_016858679.1:p.Met838Val
XM_017003191.1:c.2140A>G	XP_016858680.1:p.Met714Val
XM_017003192.1:c.1930A>G	XP_016858681.1:p.Met644Val
XM_017003193.1:c.1927A>G	XP_016858682.1:p.Met643Val
NM_001320613.2:c.2653A>G	NP_001307542.1:p.Met885Val
NM_001377128.1:c.2716A>G	NP_001364057.1:p.Met906Val
NM_001377129.1:c.2512A>G	NP_001364058.1:p.Met838Val
NM_001377130.1:c.2245A>G	NP_001364059.1:p.Met749Val
NM_001377131.1:c.1927A>G	NP_001364060.1:p.Met643Val
NM_001377132.1:c.2650A>G	NP_001364061.1:p.Met884Val
NM_004036.5:c.2650A>G MANE Select	NP_004027.2:p.Met884Val