Canonical Allele Identifier: CA425171940

Gene: ADCY3

Linked Data

• gnomAD v4: 2-24823227-G-A
• MyVariant Identifiers: chr2:g.25046096G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823227G>A , CM000664.2:g.24823227G>A	GRCh38
NC_000002.11:g.25046096G>A , CM000664.1:g.25046096G>A	GRCh37
NC_000002.10:g.24899600G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2868C>T	ENSP00000384484.2:p.Ile956=
ENST00000679454.1:c.2865C>T MANE Select	ENSP00000505261.1:p.Ile955=
ENST00000260600.9:c.2865C>T	ENSP00000260600.5:p.Ile955=
ENST00000405392.5:c.2868C>T	ENSP00000384484.2:p.Ile956=
ENST00000485887.1:n.137C>T
ENST00000606682.5:c.1806C>T	ENSP00000475652.1:p.Ile602=
NM_004036.3:c.2865C>T	NP_004027.2:p.Ile955=
XM_005264104.1:c.2868C>T	XP_005264161.1:p.Ile956=
XM_005264105.1:c.2865C>T	XP_005264162.1:p.Ile955=
XM_006711925.1:c.2934C>T	XP_006711988.1:p.Ile978=
XM_011532489.1:c.2991C>T	XP_011530791.1:p.Ile997=
XM_011532490.1:c.2988C>T	XP_011530792.1:p.Ile996=
XM_011532491.1:c.2925C>T	XP_011530793.1:p.Ile975=
XM_011532492.1:c.2991C>T	XP_011530794.1:p.Ile997=
XM_011532493.1:c.2853C>T	XP_011530795.1:p.Ile951=
XM_011532494.1:c.2793C>T	XP_011530796.1:p.Ile931=
XM_011532495.1:c.2325C>T	XP_011530797.1:p.Ile775=
XM_011532496.1:c.2268C>T	XP_011530798.1:p.Ile756=
NM_001320613.1:c.2868C>T	NP_001307542.1:p.Ile956=
NM_004036.4:c.2865C>T	NP_004027.2:p.Ile955=
XM_011532492.2:c.2991C>T	XP_011530794.1:p.Ile997=
XM_017003186.1:c.2931C>T	XP_016858675.1:p.Ile977=
XM_017003187.1:c.2922C>T	XP_016858676.1:p.Ile974=
XM_017003188.1:c.2988C>T	XP_016858677.1:p.Ile996=
XM_017003189.1:c.2850C>T	XP_016858678.1:p.Ile950=
XM_017003190.1:c.2727C>T	XP_016858679.1:p.Ile909=
XM_017003191.1:c.2355C>T	XP_016858680.1:p.Ile785=
XM_017003192.1:c.2145C>T	XP_016858681.1:p.Ile715=
XM_017003193.1:c.2142C>T	XP_016858682.1:p.Ile714=
NM_001320613.2:c.2868C>T	NP_001307542.1:p.Ile956=
NM_001377128.1:c.2931C>T	NP_001364057.1:p.Ile977=
NM_001377129.1:c.2727C>T	NP_001364058.1:p.Ile909=
NM_001377130.1:c.2332-597C>T	NP_001364059.1:n.2332-597C>T
NM_001377131.1:c.2142C>T	NP_001364060.1:p.Ile714=
NM_001377132.1:c.2865C>T	NP_001364061.1:p.Ile955=
NM_004036.5:c.2865C>T MANE Select	NP_004027.2:p.Ile955=