Canonical Allele Identifier: CA346063607

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047312A>T (hg19) ; chr2:g.24824443A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824443A>T , CM000664.2:g.24824443A>T	GRCh38
NC_000002.11:g.25047312A>T , CM000664.1:g.25047312A>T	GRCh37
NC_000002.10:g.24900816A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2674T>A	ENSP00000384484.2:p.Leu892Met
ENST00000679454.1:c.2671T>A MANE Select	ENSP00000505261.1:p.Leu891Met
ENST00000260600.9:c.2671T>A	ENSP00000260600.5:p.Leu891Met
ENST00000405392.5:c.2674T>A	ENSP00000384484.2:p.Leu892Met
ENST00000606682.5:c.1612T>A	ENSP00000475652.1:p.Leu538Met
NM_004036.3:c.2671T>A	NP_004027.2:p.Leu891Met
XM_005264104.1:c.2674T>A	XP_005264161.1:p.Leu892Met
XM_005264105.1:c.2671T>A	XP_005264162.1:p.Leu891Met
XM_006711925.1:c.2740T>A	XP_006711988.1:p.Leu914Met
XM_011532489.1:c.2797T>A	XP_011530791.1:p.Leu933Met
XM_011532490.1:c.2794T>A	XP_011530792.1:p.Leu932Met
XM_011532491.1:c.2731T>A	XP_011530793.1:p.Leu911Met
XM_011532492.1:c.2797T>A	XP_011530794.1:p.Leu933Met
XM_011532493.1:c.2659T>A	XP_011530795.1:p.Leu887Met
XM_011532494.1:c.2599T>A	XP_011530796.1:p.Leu867Met
XM_011532495.1:c.2131T>A	XP_011530797.1:p.Leu711Met
XM_011532496.1:c.2074T>A	XP_011530798.1:p.Leu692Met
NM_001320613.1:c.2674T>A	NP_001307542.1:p.Leu892Met
NM_004036.4:c.2671T>A	NP_004027.2:p.Leu891Met
XM_011532492.2:c.2797T>A	XP_011530794.1:p.Leu933Met
XM_017003186.1:c.2737T>A	XP_016858675.1:p.Leu913Met
XM_017003187.1:c.2728T>A	XP_016858676.1:p.Leu910Met
XM_017003188.1:c.2794T>A	XP_016858677.1:p.Leu932Met
XM_017003189.1:c.2656T>A	XP_016858678.1:p.Leu886Met
XM_017003190.1:c.2533T>A	XP_016858679.1:p.Leu845Met
XM_017003191.1:c.2161T>A	XP_016858680.1:p.Leu721Met
XM_017003192.1:c.1951T>A	XP_016858681.1:p.Leu651Met
XM_017003193.1:c.1948T>A	XP_016858682.1:p.Leu650Met
NM_001320613.2:c.2674T>A	NP_001307542.1:p.Leu892Met
NM_001377128.1:c.2737T>A	NP_001364057.1:p.Leu913Met
NM_001377129.1:c.2533T>A	NP_001364058.1:p.Leu845Met
NM_001377130.1:c.2266T>A	NP_001364059.1:p.Leu756Met
NM_001377131.1:c.1948T>A	NP_001364060.1:p.Leu650Met
NM_001377132.1:c.2671T>A	NP_001364061.1:p.Leu891Met
NM_004036.5:c.2671T>A MANE Select	NP_004027.2:p.Leu891Met