Canonical Allele Identifier: CA346063616

Gene: ADCY3

Linked Data

• gnomAD v4: 2-24824446-C-T
• MyVariant Identifiers: chr2:g.25047315C>T (hg19) ; chr2:g.24824446C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824446C>T , CM000664.2:g.24824446C>T	GRCh38
NC_000002.11:g.25047315C>T , CM000664.1:g.25047315C>T	GRCh37
NC_000002.10:g.24900819C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2671G>A	ENSP00000384484.2:p.Ala891Thr
ENST00000679454.1:c.2668G>A MANE Select	ENSP00000505261.1:p.Ala890Thr
ENST00000260600.9:c.2668G>A	ENSP00000260600.5:p.Ala890Thr
ENST00000405392.5:c.2671G>A	ENSP00000384484.2:p.Ala891Thr
ENST00000606682.5:c.1609G>A	ENSP00000475652.1:p.Ala537Thr
NM_004036.3:c.2668G>A	NP_004027.2:p.Ala890Thr
XM_005264104.1:c.2671G>A	XP_005264161.1:p.Ala891Thr
XM_005264105.1:c.2668G>A	XP_005264162.1:p.Ala890Thr
XM_006711925.1:c.2737G>A	XP_006711988.1:p.Ala913Thr
XM_011532489.1:c.2794G>A	XP_011530791.1:p.Ala932Thr
XM_011532490.1:c.2791G>A	XP_011530792.1:p.Ala931Thr
XM_011532491.1:c.2728G>A	XP_011530793.1:p.Ala910Thr
XM_011532492.1:c.2794G>A	XP_011530794.1:p.Ala932Thr
XM_011532493.1:c.2656G>A	XP_011530795.1:p.Ala886Thr
XM_011532494.1:c.2596G>A	XP_011530796.1:p.Ala866Thr
XM_011532495.1:c.2128G>A	XP_011530797.1:p.Ala710Thr
XM_011532496.1:c.2071G>A	XP_011530798.1:p.Ala691Thr
NM_001320613.1:c.2671G>A	NP_001307542.1:p.Ala891Thr
NM_004036.4:c.2668G>A	NP_004027.2:p.Ala890Thr
XM_011532492.2:c.2794G>A	XP_011530794.1:p.Ala932Thr
XM_017003186.1:c.2734G>A	XP_016858675.1:p.Ala912Thr
XM_017003187.1:c.2725G>A	XP_016858676.1:p.Ala909Thr
XM_017003188.1:c.2791G>A	XP_016858677.1:p.Ala931Thr
XM_017003189.1:c.2653G>A	XP_016858678.1:p.Ala885Thr
XM_017003190.1:c.2530G>A	XP_016858679.1:p.Ala844Thr
XM_017003191.1:c.2158G>A	XP_016858680.1:p.Ala720Thr
XM_017003192.1:c.1948G>A	XP_016858681.1:p.Ala650Thr
XM_017003193.1:c.1945G>A	XP_016858682.1:p.Ala649Thr
NM_001320613.2:c.2671G>A	NP_001307542.1:p.Ala891Thr
NM_001377128.1:c.2734G>A	NP_001364057.1:p.Ala912Thr
NM_001377129.1:c.2530G>A	NP_001364058.1:p.Ala844Thr
NM_001377130.1:c.2263G>A	NP_001364059.1:p.Ala755Thr
NM_001377131.1:c.1945G>A	NP_001364060.1:p.Ala649Thr
NM_001377132.1:c.2668G>A	NP_001364061.1:p.Ala890Thr
NM_004036.5:c.2668G>A MANE Select	NP_004027.2:p.Ala890Thr