Canonical Allele Identifier: CA425172026

Gene: ADCY3

Linked Data

• gnomAD v4: 2-24823341-C-T
• MyVariant Identifiers: chr2:g.25046210C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823341C>T , CM000664.2:g.24823341C>T	GRCh38
NC_000002.11:g.25046210C>T , CM000664.1:g.25046210C>T	GRCh37
NC_000002.10:g.24899714C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2754G>A	ENSP00000384484.2:p.Gln918=
ENST00000679454.1:c.2751G>A MANE Select	ENSP00000505261.1:p.Gln917=
ENST00000260600.9:c.2751G>A	ENSP00000260600.5:p.Gln917=
ENST00000405392.5:c.2754G>A	ENSP00000384484.2:p.Gln918=
ENST00000485887.1:n.23G>A
ENST00000606682.5:c.1692G>A	ENSP00000475652.1:p.Gln564=
NM_004036.3:c.2751G>A	NP_004027.2:p.Gln917=
XM_005264104.1:c.2754G>A	XP_005264161.1:p.Gln918=
XM_005264105.1:c.2751G>A	XP_005264162.1:p.Gln917=
XM_006711925.1:c.2820G>A	XP_006711988.1:p.Gln940=
XM_011532489.1:c.2877G>A	XP_011530791.1:p.Gln959=
XM_011532490.1:c.2874G>A	XP_011530792.1:p.Gln958=
XM_011532491.1:c.2811G>A	XP_011530793.1:p.Gln937=
XM_011532492.1:c.2877G>A	XP_011530794.1:p.Gln959=
XM_011532493.1:c.2739G>A	XP_011530795.1:p.Gln913=
XM_011532494.1:c.2679G>A	XP_011530796.1:p.Gln893=
XM_011532495.1:c.2211G>A	XP_011530797.1:p.Gln737=
XM_011532496.1:c.2154G>A	XP_011530798.1:p.Gln718=
NM_001320613.1:c.2754G>A	NP_001307542.1:p.Gln918=
NM_004036.4:c.2751G>A	NP_004027.2:p.Gln917=
XM_011532492.2:c.2877G>A	XP_011530794.1:p.Gln959=
XM_017003186.1:c.2817G>A	XP_016858675.1:p.Gln939=
XM_017003187.1:c.2808G>A	XP_016858676.1:p.Gln936=
XM_017003188.1:c.2874G>A	XP_016858677.1:p.Gln958=
XM_017003189.1:c.2736G>A	XP_016858678.1:p.Gln912=
XM_017003190.1:c.2613G>A	XP_016858679.1:p.Gln871=
XM_017003191.1:c.2241G>A	XP_016858680.1:p.Gln747=
XM_017003192.1:c.2031G>A	XP_016858681.1:p.Gln677=
XM_017003193.1:c.2028G>A	XP_016858682.1:p.Gln676=
NM_001320613.2:c.2754G>A	NP_001307542.1:p.Gln918=
NM_001377128.1:c.2817G>A	NP_001364057.1:p.Gln939=
NM_001377129.1:c.2613G>A	NP_001364058.1:p.Gln871=
NM_001377130.1:c.2332-711G>A	NP_001364059.1:n.2332-711G>A
NM_001377131.1:c.2028G>A	NP_001364060.1:p.Gln676=
NM_001377132.1:c.2751G>A	NP_001364061.1:p.Gln917=
NM_004036.5:c.2751G>A MANE Select	NP_004027.2:p.Gln917=