Canonical Allele Identifier: CA1398358756

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123352463C= , CM000665.2:g.123352463C=	GRCh38
NC_000003.11:g.123071310C= , CM000665.1:g.123071310C=	GRCh37
NC_000003.10:g.124554000C=	NCBI36
NG_033882.1:g.101083G=

Transcript Alleles

HGVS	Amino-acid Change
NM_183357.3:c.1253G= MANE Select	NP_899200.1:p.Arg418=
ENST00000462833.6:c.1253G= MANE Select	ENSP00000419361.1:p.Arg418=
NM_001199642.1:c.203G=	NP_001186571.1:p.Arg68=
NM_001378259.1:c.1253G=	NP_001365188.1:p.Arg418=
NM_183357.2:c.1253G=	NP_899200.1:p.Arg418=
ENST00000309879.9:c.203G=	ENSP00000308685.5:p.Arg68=
ENST00000462833.5:c.1253G=	ENSP00000419361.1:p.Arg418=
ENST00000466617.5:c.-71G=	ENSP00000420082.1:n.-71G=
ENST00000466617.6:c.-71G=	ENSP00000420082.2:n.-71G=
ENST00000470367.1:n.548G=
ENST00000470367.2:c.218G=	ENSP00000514541.1:p.Arg73=
ENST00000476455.1:c.157G=	ENSP00000417789.1:p.Gly53=
ENST00000483566.1:c.-71G=	ENSP00000420252.1:n.-71G=
ENST00000483566.2:c.-71G=	ENSP00000420252.2:n.-71G=
ENST00000491190.5:c.152G=	ENSP00000418537.1:p.Arg51=
ENST00000699714.1:c.-71G=	ENSP00000514539.1:n.-71G=
ENST00000699715.1:c.-71G=	ENSP00000514540.1:n.-71G=
ENST00000699716.1:c.-71G=	ENSP00000514542.1:n.-71G=
ENST00000699718.1:c.1253G=	ENSP00000514543.1:p.Arg418=
XM_005247077.2:c.1253G=	XP_005247134.1:p.Arg418=
XM_005247077.4:c.1253G=	XP_005247134.1:p.Arg418=
XM_005247078.1:c.203G=	XP_005247135.1:p.Arg68=
XM_006713483.1:c.152G=	XP_006713546.1:p.Arg51=
XM_006713484.1:c.-71G=	XP_006713547.1:n.-71G=
XM_011512358.1:c.1253G=	XP_011510660.1:p.Arg418=
XM_011512359.1:c.254G=	XP_011510661.1:p.Arg85=
XM_011512359.2:c.254G=	XP_011510661.1:p.Arg85=
XM_011512360.1:c.164G=	XP_011510662.1:p.Arg55=
XM_011512360.3:c.164G=	XP_011510662.1:p.Arg55=
XM_011512361.1:c.-71G=	XP_011510663.1:n.-71G=
XM_017005638.1:c.155G=	XP_016861127.1:p.Arg52=
XM_017005639.1:c.155G=	XP_016861128.1:p.Arg52=