Canonical Allele Identifier: CA1398330409

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291247G= , CM000665.2:g.123291247G=	GRCh38
NC_000003.11:g.123010094G= , CM000665.1:g.123010094G=	GRCh37
NC_000003.10:g.124492784G=	NCBI36
NG_033882.1:g.162299C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1870C=	ENSP00000420082.2:p.Gln624=
ENST00000470367.2:c.2158C=	ENSP00000514541.1:p.Gln720=
ENST00000483566.2:c.1870C=	ENSP00000420252.2:p.Gln624=
ENST00000699714.1:c.1870C=	ENSP00000514539.1:p.Gln624=
ENST00000699715.1:c.1870C=	ENSP00000514540.1:p.Gln624=
ENST00000699716.1:c.1870C=	ENSP00000514542.1:p.Gln624=
ENST00000699717.1:n.1596C=
ENST00000699718.1:c.3268C=	ENSP00000514543.1:p.Gln1090=
ENST00000462833.6:c.3193C= MANE Select	ENSP00000419361.1:p.Gln1065=
ENST00000309879.9:c.2143C=	ENSP00000308685.5:p.Gln715=
ENST00000462833.5:c.3193C=	ENSP00000419361.1:p.Gln1065=
ENST00000491190.5:c.2167C=	ENSP00000418537.1:p.Gln723=
NM_001199642.1:c.2143C=	NP_001186571.1:p.Gln715=
NM_183357.2:c.3193C=	NP_899200.1:p.Gln1065=
XM_005247077.2:c.3268C=	XP_005247134.1:p.Gln1090=
XM_005247078.1:c.2218C=	XP_005247135.1:p.Gln740=
XM_006713483.1:c.2167C=	XP_006713546.1:p.Gln723=
XM_006713484.1:c.1945C=	XP_006713547.1:p.Gln649=
XM_011512359.1:c.2269C=	XP_011510661.1:p.Gln757=
XM_011512360.1:c.2179C=	XP_011510662.1:p.Gln727=
XM_011512361.1:c.1945C=	XP_011510663.1:p.Gln649=
XM_005247077.4:c.3268C=	XP_005247134.1:p.Gln1090=
XM_011512359.2:c.2269C=	XP_011510661.1:p.Gln757=
XM_011512360.3:c.2179C=	XP_011510662.1:p.Gln727=
XM_017005638.1:c.2170C=	XP_016861127.1:p.Gln724=
XM_017005639.1:c.2170C=	XP_016861128.1:p.Gln724=
NM_001378259.1:c.3268C=	NP_001365188.1:p.Gln1090=
NM_183357.3:c.3193C= MANE Select	NP_899200.1:p.Gln1065=