Canonical Allele Identifier: CA346062852

Gene: ADCY3

Linked Data

• dbSNP Id: rs2148371661
• MyVariant Identifiers: chr2:g.25046163G>A (hg19) ; chr2:g.24823294G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823294G>A , CM000664.2:g.24823294G>A	GRCh38
NC_000002.11:g.25046163G>A , CM000664.1:g.25046163G>A	GRCh37
NC_000002.10:g.24899667G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2801C>T	ENSP00000384484.2:p.Ala934Val
ENST00000679454.1:c.2798C>T MANE Select	ENSP00000505261.1:p.Ala933Val
ENST00000260600.9:c.2798C>T	ENSP00000260600.5:p.Ala933Val
ENST00000405392.5:c.2801C>T	ENSP00000384484.2:p.Ala934Val
ENST00000485887.1:n.70C>T
ENST00000606682.5:c.1739C>T	ENSP00000475652.1:p.Ala580Val
NM_004036.3:c.2798C>T	NP_004027.2:p.Ala933Val
XM_005264104.1:c.2801C>T	XP_005264161.1:p.Ala934Val
XM_005264105.1:c.2798C>T	XP_005264162.1:p.Ala933Val
XM_006711925.1:c.2867C>T	XP_006711988.1:p.Ala956Val
XM_011532489.1:c.2924C>T	XP_011530791.1:p.Ala975Val
XM_011532490.1:c.2921C>T	XP_011530792.1:p.Ala974Val
XM_011532491.1:c.2858C>T	XP_011530793.1:p.Ala953Val
XM_011532492.1:c.2924C>T	XP_011530794.1:p.Ala975Val
XM_011532493.1:c.2786C>T	XP_011530795.1:p.Ala929Val
XM_011532494.1:c.2726C>T	XP_011530796.1:p.Ala909Val
XM_011532495.1:c.2258C>T	XP_011530797.1:p.Ala753Val
XM_011532496.1:c.2201C>T	XP_011530798.1:p.Ala734Val
NM_001320613.1:c.2801C>T	NP_001307542.1:p.Ala934Val
NM_004036.4:c.2798C>T	NP_004027.2:p.Ala933Val
XM_011532492.2:c.2924C>T	XP_011530794.1:p.Ala975Val
XM_017003186.1:c.2864C>T	XP_016858675.1:p.Ala955Val
XM_017003187.1:c.2855C>T	XP_016858676.1:p.Ala952Val
XM_017003188.1:c.2921C>T	XP_016858677.1:p.Ala974Val
XM_017003189.1:c.2783C>T	XP_016858678.1:p.Ala928Val
XM_017003190.1:c.2660C>T	XP_016858679.1:p.Ala887Val
XM_017003191.1:c.2288C>T	XP_016858680.1:p.Ala763Val
XM_017003192.1:c.2078C>T	XP_016858681.1:p.Ala693Val
XM_017003193.1:c.2075C>T	XP_016858682.1:p.Ala692Val
NM_001320613.2:c.2801C>T	NP_001307542.1:p.Ala934Val
NM_001377128.1:c.2864C>T	NP_001364057.1:p.Ala955Val
NM_001377129.1:c.2660C>T	NP_001364058.1:p.Ala887Val
NM_001377130.1:c.2332-664C>T	NP_001364059.1:n.2332-664C>T
NM_001377131.1:c.2075C>T	NP_001364060.1:p.Ala692Val
NM_001377132.1:c.2798C>T	NP_001364061.1:p.Ala933Val
NM_004036.5:c.2798C>T MANE Select	NP_004027.2:p.Ala933Val