Canonical Allele Identifier: CA1398346267

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123325411T= , CM000665.2:g.123325411T=	GRCh38
NC_000003.11:g.123044258T= , CM000665.1:g.123044258T=	GRCh37
NC_000003.10:g.124526948T=	NCBI36
NG_033882.1:g.128135A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.676A=	ENSP00000420082.2:p.Ile226=
ENST00000470367.2:c.964A=	ENSP00000514541.1:p.Ile322=
ENST00000483566.2:c.676A=	ENSP00000420252.2:p.Ile226=
ENST00000699714.1:c.676A=	ENSP00000514539.1:p.Ile226=
ENST00000699715.1:c.676A=	ENSP00000514540.1:p.Ile226=
ENST00000699716.1:c.676A=	ENSP00000514542.1:p.Ile226=
ENST00000699718.1:c.1999A=	ENSP00000514543.1:p.Ile667=
ENST00000699719.1:n.258A=
ENST00000462833.6:c.1999A= MANE Select	ENSP00000419361.1:p.Ile667=
ENST00000309879.9:c.949A=	ENSP00000308685.5:p.Ile317=
ENST00000462833.5:c.1999A=	ENSP00000419361.1:p.Ile667=
ENST00000466617.5:c.676A=	ENSP00000420082.1:p.Ile226=
ENST00000491190.5:c.898A=	ENSP00000418537.1:p.Ile300=
NM_001199642.1:c.949A=	NP_001186571.1:p.Ile317=
NM_183357.2:c.1999A=	NP_899200.1:p.Ile667=
XM_005247077.2:c.1999A=	XP_005247134.1:p.Ile667=
XM_005247078.1:c.949A=	XP_005247135.1:p.Ile317=
XM_006713483.1:c.898A=	XP_006713546.1:p.Ile300=
XM_006713484.1:c.676A=	XP_006713547.1:p.Ile226=
XM_011512358.1:c.1999A=	XP_011510660.1:p.Ile667=
XM_011512359.1:c.1000A=	XP_011510661.1:p.Ile334=
XM_011512360.1:c.910A=	XP_011510662.1:p.Ile304=
XM_011512361.1:c.676A=	XP_011510663.1:p.Ile226=
XM_005247077.4:c.1999A=	XP_005247134.1:p.Ile667=
XM_011512359.2:c.1000A=	XP_011510661.1:p.Ile334=
XM_011512360.3:c.910A=	XP_011510662.1:p.Ile304=
XM_017005638.1:c.901A=	XP_016861127.1:p.Ile301=
XM_017005639.1:c.901A=	XP_016861128.1:p.Ile301=
NM_001378259.1:c.1999A=	NP_001365188.1:p.Ile667=
NM_183357.3:c.1999A= MANE Select	NP_899200.1:p.Ile667=