Canonical Allele Identifier: CA1398346235

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123325348G= , CM000665.2:g.123325348G=	GRCh38
NC_000003.11:g.123044195G= , CM000665.1:g.123044195G=	GRCh37
NC_000003.10:g.124526885G=	NCBI36
NG_033882.1:g.128198C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.739C=	ENSP00000420082.2:p.Gln247=
ENST00000470367.2:c.1027C=	ENSP00000514541.1:p.Gln343=
ENST00000483566.2:c.739C=	ENSP00000420252.2:p.Gln247=
ENST00000699714.1:c.739C=	ENSP00000514539.1:p.Gln247=
ENST00000699715.1:c.739C=	ENSP00000514540.1:p.Gln247=
ENST00000699716.1:c.739C=	ENSP00000514542.1:p.Gln247=
ENST00000699718.1:c.2062C=	ENSP00000514543.1:p.Gln688=
ENST00000699719.1:n.321C=
ENST00000462833.6:c.2062C= MANE Select	ENSP00000419361.1:p.Gln688=
ENST00000309879.9:c.1012C=	ENSP00000308685.5:p.Gln338=
ENST00000462833.5:c.2062C=	ENSP00000419361.1:p.Gln688=
ENST00000466617.5:c.739C=	ENSP00000420082.1:p.Gln247=
ENST00000491190.5:c.961C=	ENSP00000418537.1:p.Gln321=
NM_001199642.1:c.1012C=	NP_001186571.1:p.Gln338=
NM_183357.2:c.2062C=	NP_899200.1:p.Gln688=
XM_005247077.2:c.2062C=	XP_005247134.1:p.Gln688=
XM_005247078.1:c.1012C=	XP_005247135.1:p.Gln338=
XM_006713483.1:c.961C=	XP_006713546.1:p.Gln321=
XM_006713484.1:c.739C=	XP_006713547.1:p.Gln247=
XM_011512358.1:c.2062C=	XP_011510660.1:p.Gln688=
XM_011512359.1:c.1063C=	XP_011510661.1:p.Gln355=
XM_011512360.1:c.973C=	XP_011510662.1:p.Gln325=
XM_011512361.1:c.739C=	XP_011510663.1:p.Gln247=
XM_005247077.4:c.2062C=	XP_005247134.1:p.Gln688=
XM_011512359.2:c.1063C=	XP_011510661.1:p.Gln355=
XM_011512360.3:c.973C=	XP_011510662.1:p.Gln325=
XM_017005638.1:c.964C=	XP_016861127.1:p.Gln322=
XM_017005639.1:c.964C=	XP_016861128.1:p.Gln322=
NM_001378259.1:c.2062C=	NP_001365188.1:p.Gln688=
NM_183357.3:c.2062C= MANE Select	NP_899200.1:p.Gln688=