Canonical Allele Identifier: CA435293212

Gene: ADCY5

Linked Data

• gnomAD v4: 3-123319809-C-T
• MyVariant Identifiers: chr3:g.123038656C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123319809C>T , CM000665.2:g.123319809C>T	GRCh38
NC_000003.11:g.123038656C>T , CM000665.1:g.123038656C>T	GRCh37
NC_000003.10:g.124521346C>T	NCBI36
NG_033882.1:g.133737G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.798G>A	ENSP00000420082.2:p.Gln266=
ENST00000470367.2:c.1086G>A	ENSP00000514541.1:p.Gln362=
ENST00000483566.2:c.798G>A	ENSP00000420252.2:p.Gln266=
ENST00000699714.1:c.798G>A	ENSP00000514539.1:p.Gln266=
ENST00000699715.1:c.798G>A	ENSP00000514540.1:p.Gln266=
ENST00000699716.1:c.798G>A	ENSP00000514542.1:p.Gln266=
ENST00000699718.1:c.2121G>A	ENSP00000514543.1:p.Gln707=
ENST00000699719.1:n.380G>A
ENST00000462833.6:c.2121G>A MANE Select	ENSP00000419361.1:p.Gln707=
ENST00000309879.9:c.1071G>A	ENSP00000308685.5:p.Gln357=
ENST00000462833.5:c.2121G>A	ENSP00000419361.1:p.Gln707=
ENST00000466617.5:c.798G>A	ENSP00000420082.1:p.Gln266=
ENST00000491190.5:c.1020G>A	ENSP00000418537.1:p.Gln340=
NM_001199642.1:c.1071G>A	NP_001186571.1:p.Gln357=
NM_183357.2:c.2121G>A	NP_899200.1:p.Gln707=
XM_005247077.2:c.2121G>A	XP_005247134.1:p.Gln707=
XM_005247078.1:c.1071G>A	XP_005247135.1:p.Gln357=
XM_006713483.1:c.1020G>A	XP_006713546.1:p.Gln340=
XM_006713484.1:c.798G>A	XP_006713547.1:p.Gln266=
XM_011512358.1:c.2121G>A	XP_011510660.1:p.Gln707=
XM_011512359.1:c.1122G>A	XP_011510661.1:p.Gln374=
XM_011512360.1:c.1032G>A	XP_011510662.1:p.Gln344=
XM_011512361.1:c.798G>A	XP_011510663.1:p.Gln266=
XM_005247077.4:c.2121G>A	XP_005247134.1:p.Gln707=
XM_011512359.2:c.1122G>A	XP_011510661.1:p.Gln374=
XM_011512360.3:c.1032G>A	XP_011510662.1:p.Gln344=
XM_017005638.1:c.1023G>A	XP_016861127.1:p.Gln341=
XM_017005639.1:c.1023G>A	XP_016861128.1:p.Gln341=
NM_001378259.1:c.2121G>A	NP_001365188.1:p.Gln707=
NM_183357.3:c.2121G>A MANE Select	NP_899200.1:p.Gln707=