Canonical Allele Identifier: CA1398327444

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284620G= , CM000665.2:g.123284620G=	GRCh38
NC_000003.11:g.123003467G= , CM000665.1:g.123003467G=	GRCh37
NC_000003.10:g.124486157G=	NCBI36
NG_033882.1:g.168926C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2451C=	ENSP00000420082.2:p.Pro817=
ENST00000470367.2:c.2739C=	ENSP00000514541.1:p.Pro913=
ENST00000483566.2:c.2451C=	ENSP00000420252.2:p.Pro817=
ENST00000699714.1:c.2451C=	ENSP00000514539.1:p.Pro817=
ENST00000699715.1:c.2451C=	ENSP00000514540.1:p.Pro817=
ENST00000699716.1:c.2451C=	ENSP00000514542.1:p.Pro817=
ENST00000699717.1:n.2177C=
ENST00000699718.1:c.3849C=	ENSP00000514543.1:p.Pro1283=
ENST00000462833.6:c.3774C= MANE Select	ENSP00000419361.1:p.Pro1258=
ENST00000309879.9:c.2724C=	ENSP00000308685.5:p.Pro908=
ENST00000462833.5:c.3774C=	ENSP00000419361.1:p.Pro1258=
ENST00000478092.1:n.544C=
ENST00000491190.5:c.2748C=	ENSP00000418537.1:p.Pro916=
NM_001199642.1:c.2724C=	NP_001186571.1:p.Pro908=
NM_183357.2:c.3774C=	NP_899200.1:p.Pro1258=
XM_005247077.2:c.3849C=	XP_005247134.1:p.Pro1283=
XM_005247078.1:c.2799C=	XP_005247135.1:p.Pro933=
XM_006713483.1:c.2748C=	XP_006713546.1:p.Pro916=
XM_006713484.1:c.2526C=	XP_006713547.1:p.Pro842=
XM_011512359.1:c.2850C=	XP_011510661.1:p.Pro950=
XM_011512360.1:c.2760C=	XP_011510662.1:p.Pro920=
XM_011512361.1:c.2526C=	XP_011510663.1:p.Pro842=
XM_005247077.4:c.3849C=	XP_005247134.1:p.Pro1283=
XM_011512359.2:c.2850C=	XP_011510661.1:p.Pro950=
XM_011512360.3:c.2760C=	XP_011510662.1:p.Pro920=
XM_017005638.1:c.2751C=	XP_016861127.1:p.Pro917=
XM_017005639.1:c.2751C=	XP_016861128.1:p.Pro917=
NM_001378259.1:c.3849C=	NP_001365188.1:p.Pro1283=
NM_183357.3:c.3774C= MANE Select	NP_899200.1:p.Pro1258=