Canonical Allele Identifier: CA1398347266

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123332657G= , CM000665.2:g.123332657G=	GRCh38
NC_000003.11:g.123051504G= , CM000665.1:g.123051504G=	GRCh37
NC_000003.10:g.124534194G=	NCBI36
NG_033882.1:g.120889C=

Transcript Alleles

HGVS	Amino-acid Change
NM_183357.3:c.1425C= MANE Select	NP_899200.1:p.Ile475=
ENST00000462833.6:c.1425C= MANE Select	ENSP00000419361.1:p.Ile475=
NM_001199642.1:c.375C=	NP_001186571.1:p.Ile125=
NM_001378259.1:c.1425C=	NP_001365188.1:p.Ile475=
NM_183357.2:c.1425C=	NP_899200.1:p.Ile475=
ENST00000309879.9:c.375C=	ENSP00000308685.5:p.Ile125=
ENST00000462833.5:c.1425C=	ENSP00000419361.1:p.Ile475=
ENST00000466617.5:c.102C=	ENSP00000420082.1:p.Ile34=
ENST00000466617.6:c.102C=	ENSP00000420082.2:p.Ile34=
ENST00000470367.2:c.390C=	ENSP00000514541.1:p.Ile130=
ENST00000476455.1:c.*92C=	ENSP00000417789.1:n.*92C=
ENST00000483566.1:c.102C=	ENSP00000420252.1:p.Ile34=
ENST00000483566.2:c.102C=	ENSP00000420252.2:p.Ile34=
ENST00000491190.5:c.324C=	ENSP00000418537.1:p.Ile108=
ENST00000699714.1:c.102C=	ENSP00000514539.1:p.Ile34=
ENST00000699715.1:c.102C=	ENSP00000514540.1:p.Ile34=
ENST00000699716.1:c.102C=	ENSP00000514542.1:p.Ile34=
ENST00000699718.1:c.1425C=	ENSP00000514543.1:p.Ile475=
XM_005247077.2:c.1425C=	XP_005247134.1:p.Ile475=
XM_005247077.4:c.1425C=	XP_005247134.1:p.Ile475=
XM_005247078.1:c.375C=	XP_005247135.1:p.Ile125=
XM_006713483.1:c.324C=	XP_006713546.1:p.Ile108=
XM_006713484.1:c.102C=	XP_006713547.1:p.Ile34=
XM_011512358.1:c.1425C=	XP_011510660.1:p.Ile475=
XM_011512359.1:c.426C=	XP_011510661.1:p.Ile142=
XM_011512359.2:c.426C=	XP_011510661.1:p.Ile142=
XM_011512360.1:c.336C=	XP_011510662.1:p.Ile112=
XM_011512360.3:c.336C=	XP_011510662.1:p.Ile112=
XM_011512361.1:c.102C=	XP_011510663.1:p.Ile34=
XM_017005638.1:c.327C=	XP_016861127.1:p.Ile109=
XM_017005639.1:c.327C=	XP_016861128.1:p.Ile109=