Canonical Allele Identifier: CA435297655

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123003470C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284623C>A , CM000665.2:g.123284623C>A	GRCh38
NC_000003.11:g.123003470C>A , CM000665.1:g.123003470C>A	GRCh37
NC_000003.10:g.124486160C>A	NCBI36
NG_033882.1:g.168923G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2448G>T	ENSP00000420082.2:p.Gly816=
ENST00000470367.2:c.2736G>T	ENSP00000514541.1:p.Gly912=
ENST00000483566.2:c.2448G>T	ENSP00000420252.2:p.Gly816=
ENST00000699714.1:c.2448G>T	ENSP00000514539.1:p.Gly816=
ENST00000699715.1:c.2448G>T	ENSP00000514540.1:p.Gly816=
ENST00000699716.1:c.2448G>T	ENSP00000514542.1:p.Gly816=
ENST00000699717.1:n.2174G>T
ENST00000699718.1:c.3846G>T	ENSP00000514543.1:p.Gly1282=
ENST00000462833.6:c.3771G>T MANE Select	ENSP00000419361.1:p.Gly1257=
ENST00000309879.9:c.2721G>T	ENSP00000308685.5:p.Gly907=
ENST00000462833.5:c.3771G>T	ENSP00000419361.1:p.Gly1257=
ENST00000478092.1:n.541G>T
ENST00000491190.5:c.2745G>T	ENSP00000418537.1:p.Gly915=
NM_001199642.1:c.2721G>T	NP_001186571.1:p.Gly907=
NM_183357.2:c.3771G>T	NP_899200.1:p.Gly1257=
XM_005247077.2:c.3846G>T	XP_005247134.1:p.Gly1282=
XM_005247078.1:c.2796G>T	XP_005247135.1:p.Gly932=
XM_006713483.1:c.2745G>T	XP_006713546.1:p.Gly915=
XM_006713484.1:c.2523G>T	XP_006713547.1:p.Gly841=
XM_011512359.1:c.2847G>T	XP_011510661.1:p.Gly949=
XM_011512360.1:c.2757G>T	XP_011510662.1:p.Gly919=
XM_011512361.1:c.2523G>T	XP_011510663.1:p.Gly841=
XM_005247077.4:c.3846G>T	XP_005247134.1:p.Gly1282=
XM_011512359.2:c.2847G>T	XP_011510661.1:p.Gly949=
XM_011512360.3:c.2757G>T	XP_011510662.1:p.Gly919=
XM_017005638.1:c.2748G>T	XP_016861127.1:p.Gly916=
XM_017005639.1:c.2748G>T	XP_016861128.1:p.Gly916=
NM_001378259.1:c.3846G>T	NP_001365188.1:p.Gly1282=
NM_183357.3:c.3771G>T MANE Select	NP_899200.1:p.Gly1257=