Canonical Allele Identifier: CA1398330369

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291138T= , CM000665.2:g.123291138T=	GRCh38
NC_000003.11:g.123009985T= , CM000665.1:g.123009985T=	GRCh37
NC_000003.10:g.124492675T=	NCBI36
NG_033882.1:g.162408A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1979A=	ENSP00000420082.2:p.Asn660=
ENST00000470367.2:c.2267A=	ENSP00000514541.1:p.Asn756=
ENST00000483566.2:c.1979A=	ENSP00000420252.2:p.Asn660=
ENST00000699714.1:c.1979A=	ENSP00000514539.1:p.Asn660=
ENST00000699715.1:c.1979A=	ENSP00000514540.1:p.Asn660=
ENST00000699716.1:c.1979A=	ENSP00000514542.1:p.Asn660=
ENST00000699717.1:n.1705A=
ENST00000699718.1:c.3377A=	ENSP00000514543.1:p.Asn1126=
ENST00000462833.6:c.3302A= MANE Select	ENSP00000419361.1:p.Asn1101=
ENST00000309879.9:c.2252A=	ENSP00000308685.5:p.Asn751=
ENST00000462833.5:c.3302A=	ENSP00000419361.1:p.Asn1101=
ENST00000491190.5:c.2276A=	ENSP00000418537.1:p.Asn759=
NM_001199642.1:c.2252A=	NP_001186571.1:p.Asn751=
NM_183357.2:c.3302A=	NP_899200.1:p.Asn1101=
XM_005247077.2:c.3377A=	XP_005247134.1:p.Asn1126=
XM_005247078.1:c.2327A=	XP_005247135.1:p.Asn776=
XM_006713483.1:c.2276A=	XP_006713546.1:p.Asn759=
XM_006713484.1:c.2054A=	XP_006713547.1:p.Asn685=
XM_011512359.1:c.2378A=	XP_011510661.1:p.Asn793=
XM_011512360.1:c.2288A=	XP_011510662.1:p.Asn763=
XM_011512361.1:c.2054A=	XP_011510663.1:p.Asn685=
XM_005247077.4:c.3377A=	XP_005247134.1:p.Asn1126=
XM_011512359.2:c.2378A=	XP_011510661.1:p.Asn793=
XM_011512360.3:c.2288A=	XP_011510662.1:p.Asn763=
XM_017005638.1:c.2279A=	XP_016861127.1:p.Asn760=
XM_017005639.1:c.2279A=	XP_016861128.1:p.Asn760=
NM_001378259.1:c.3377A=	NP_001365188.1:p.Asn1126=
NM_183357.3:c.3302A= MANE Select	NP_899200.1:p.Asn1101=