Canonical Allele Identifier: CA346062686

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046137T>C (hg19) ; chr2:g.24823268T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823268T>C , CM000664.2:g.24823268T>C	GRCh38
NC_000002.11:g.25046137T>C , CM000664.1:g.25046137T>C	GRCh37
NC_000002.10:g.24899641T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2827A>G	ENSP00000384484.2:p.Asn943Asp
ENST00000679454.1:c.2824A>G MANE Select	ENSP00000505261.1:p.Asn942Asp
ENST00000260600.9:c.2824A>G	ENSP00000260600.5:p.Asn942Asp
ENST00000405392.5:c.2827A>G	ENSP00000384484.2:p.Asn943Asp
ENST00000485887.1:n.96A>G
ENST00000606682.5:c.1765A>G	ENSP00000475652.1:p.Asn589Asp
NM_004036.3:c.2824A>G	NP_004027.2:p.Asn942Asp
XM_005264104.1:c.2827A>G	XP_005264161.1:p.Asn943Asp
XM_005264105.1:c.2824A>G	XP_005264162.1:p.Asn942Asp
XM_006711925.1:c.2893A>G	XP_006711988.1:p.Asn965Asp
XM_011532489.1:c.2950A>G	XP_011530791.1:p.Asn984Asp
XM_011532490.1:c.2947A>G	XP_011530792.1:p.Asn983Asp
XM_011532491.1:c.2884A>G	XP_011530793.1:p.Asn962Asp
XM_011532492.1:c.2950A>G	XP_011530794.1:p.Asn984Asp
XM_011532493.1:c.2812A>G	XP_011530795.1:p.Asn938Asp
XM_011532494.1:c.2752A>G	XP_011530796.1:p.Asn918Asp
XM_011532495.1:c.2284A>G	XP_011530797.1:p.Asn762Asp
XM_011532496.1:c.2227A>G	XP_011530798.1:p.Asn743Asp
NM_001320613.1:c.2827A>G	NP_001307542.1:p.Asn943Asp
NM_004036.4:c.2824A>G	NP_004027.2:p.Asn942Asp
XM_011532492.2:c.2950A>G	XP_011530794.1:p.Asn984Asp
XM_017003186.1:c.2890A>G	XP_016858675.1:p.Asn964Asp
XM_017003187.1:c.2881A>G	XP_016858676.1:p.Asn961Asp
XM_017003188.1:c.2947A>G	XP_016858677.1:p.Asn983Asp
XM_017003189.1:c.2809A>G	XP_016858678.1:p.Asn937Asp
XM_017003190.1:c.2686A>G	XP_016858679.1:p.Asn896Asp
XM_017003191.1:c.2314A>G	XP_016858680.1:p.Asn772Asp
XM_017003192.1:c.2104A>G	XP_016858681.1:p.Asn702Asp
XM_017003193.1:c.2101A>G	XP_016858682.1:p.Asn701Asp
NM_001320613.2:c.2827A>G	NP_001307542.1:p.Asn943Asp
NM_001377128.1:c.2890A>G	NP_001364057.1:p.Asn964Asp
NM_001377129.1:c.2686A>G	NP_001364058.1:p.Asn896Asp
NM_001377130.1:c.2332-638A>G	NP_001364059.1:n.2332-638A>G
NM_001377131.1:c.2101A>G	NP_001364060.1:p.Asn701Asp
NM_001377132.1:c.2824A>G	NP_001364061.1:p.Asn942Asp
NM_004036.5:c.2824A>G MANE Select	NP_004027.2:p.Asn942Asp