Canonical Allele Identifier: CA346063599

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047310C>G (hg19) ; chr2:g.24824441C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824441C>G , CM000664.2:g.24824441C>G	GRCh38
NC_000002.11:g.25047310C>G , CM000664.1:g.25047310C>G	GRCh37
NC_000002.10:g.24900814C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2676G>C	ENSP00000384484.2:p.Leu892Phe
ENST00000679454.1:c.2673G>C MANE Select	ENSP00000505261.1:p.Leu891Phe
ENST00000260600.9:c.2673G>C	ENSP00000260600.5:p.Leu891Phe
ENST00000405392.5:c.2676G>C	ENSP00000384484.2:p.Leu892Phe
ENST00000606682.5:c.1614G>C	ENSP00000475652.1:p.Leu538Phe
NM_004036.3:c.2673G>C	NP_004027.2:p.Leu891Phe
XM_005264104.1:c.2676G>C	XP_005264161.1:p.Leu892Phe
XM_005264105.1:c.2673G>C	XP_005264162.1:p.Leu891Phe
XM_006711925.1:c.2742G>C	XP_006711988.1:p.Leu914Phe
XM_011532489.1:c.2799G>C	XP_011530791.1:p.Leu933Phe
XM_011532490.1:c.2796G>C	XP_011530792.1:p.Leu932Phe
XM_011532491.1:c.2733G>C	XP_011530793.1:p.Leu911Phe
XM_011532492.1:c.2799G>C	XP_011530794.1:p.Leu933Phe
XM_011532493.1:c.2661G>C	XP_011530795.1:p.Leu887Phe
XM_011532494.1:c.2601G>C	XP_011530796.1:p.Leu867Phe
XM_011532495.1:c.2133G>C	XP_011530797.1:p.Leu711Phe
XM_011532496.1:c.2076G>C	XP_011530798.1:p.Leu692Phe
NM_001320613.1:c.2676G>C	NP_001307542.1:p.Leu892Phe
NM_004036.4:c.2673G>C	NP_004027.2:p.Leu891Phe
XM_011532492.2:c.2799G>C	XP_011530794.1:p.Leu933Phe
XM_017003186.1:c.2739G>C	XP_016858675.1:p.Leu913Phe
XM_017003187.1:c.2730G>C	XP_016858676.1:p.Leu910Phe
XM_017003188.1:c.2796G>C	XP_016858677.1:p.Leu932Phe
XM_017003189.1:c.2658G>C	XP_016858678.1:p.Leu886Phe
XM_017003190.1:c.2535G>C	XP_016858679.1:p.Leu845Phe
XM_017003191.1:c.2163G>C	XP_016858680.1:p.Leu721Phe
XM_017003192.1:c.1953G>C	XP_016858681.1:p.Leu651Phe
XM_017003193.1:c.1950G>C	XP_016858682.1:p.Leu650Phe
NM_001320613.2:c.2676G>C	NP_001307542.1:p.Leu892Phe
NM_001377128.1:c.2739G>C	NP_001364057.1:p.Leu913Phe
NM_001377129.1:c.2535G>C	NP_001364058.1:p.Leu845Phe
NM_001377130.1:c.2268G>C	NP_001364059.1:p.Leu756Phe
NM_001377131.1:c.1950G>C	NP_001364060.1:p.Leu650Phe
NM_001377132.1:c.2673G>C	NP_001364061.1:p.Leu891Phe
NM_004036.5:c.2673G>C MANE Select	NP_004027.2:p.Leu891Phe